EP3040439B1 - Hot-rolled steel sheet and method for manufacturing the same - Google Patents

Hot-rolled steel sheet and method for manufacturing the same Download PDF

Info

Publication number
EP3040439B1
EP3040439B1 EP14866276.0A EP14866276A EP3040439B1 EP 3040439 B1 EP3040439 B1 EP 3040439B1 EP 14866276 A EP14866276 A EP 14866276A EP 3040439 B1 EP3040439 B1 EP 3040439B1
Authority
EP
European Patent Office
Prior art keywords
less
steel sheet
hot
rolled steel
temperature
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
EP14866276.0A
Other languages
German (de)
French (fr)
Other versions
EP3040439A4 (en
EP3040439A1 (en
Inventor
Tomoaki Shibata
Sota GOTO
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
JFE Steel Corp
Original Assignee
JFE Steel Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by JFE Steel Corp filed Critical JFE Steel Corp
Publication of EP3040439A1 publication Critical patent/EP3040439A1/en
Publication of EP3040439A4 publication Critical patent/EP3040439A4/en
Application granted granted Critical
Publication of EP3040439B1 publication Critical patent/EP3040439B1/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/38Ferrous alloys, e.g. steel alloys containing chromium with more than 1.5% by weight of manganese
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D6/00Heat treatment of ferrous alloys
    • C21D6/005Heat treatment of ferrous alloys containing Mn
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D6/00Heat treatment of ferrous alloys
    • C21D6/008Heat treatment of ferrous alloys containing Si
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D8/00Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/02Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D8/00Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/02Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • C21D8/0221Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the working steps
    • C21D8/0226Hot rolling
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D8/00Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/02Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • C21D8/0247Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the heat treatment
    • C21D8/0263Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the heat treatment following hot rolling
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D8/00Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/06Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of rods or wires
    • C21D8/065Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of rods or wires of ferrous alloys
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D9/00Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
    • C21D9/08Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for tubular bodies or pipes
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D9/00Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
    • C21D9/46Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for sheet metals
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/001Ferrous alloys, e.g. steel alloys containing N
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/002Ferrous alloys, e.g. steel alloys containing In, Mg, or other elements not provided for in one single group C22C38/001 - C22C38/60
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/02Ferrous alloys, e.g. steel alloys containing silicon
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/04Ferrous alloys, e.g. steel alloys containing manganese
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/06Ferrous alloys, e.g. steel alloys containing aluminium
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/22Ferrous alloys, e.g. steel alloys containing chromium with molybdenum or tungsten
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/24Ferrous alloys, e.g. steel alloys containing chromium with vanadium
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/26Ferrous alloys, e.g. steel alloys containing chromium with niobium or tantalum
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/28Ferrous alloys, e.g. steel alloys containing chromium with titanium or zirconium
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/32Ferrous alloys, e.g. steel alloys containing chromium with boron
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/40Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • C22C38/42Ferrous alloys, e.g. steel alloys containing chromium with nickel with copper
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/40Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • C22C38/44Ferrous alloys, e.g. steel alloys containing chromium with nickel with molybdenum or tungsten
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/40Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • C22C38/46Ferrous alloys, e.g. steel alloys containing chromium with nickel with vanadium
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/40Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • C22C38/48Ferrous alloys, e.g. steel alloys containing chromium with nickel with niobium or tantalum
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/40Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • C22C38/50Ferrous alloys, e.g. steel alloys containing chromium with nickel with titanium or zirconium
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/40Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • C22C38/54Ferrous alloys, e.g. steel alloys containing chromium with nickel with boron
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/40Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • C22C38/58Ferrous alloys, e.g. steel alloys containing chromium with nickel with more than 1.5% by weight of manganese
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D2211/00Microstructure comprising significant phases
    • C21D2211/001Austenite
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D2211/00Microstructure comprising significant phases
    • C21D2211/002Bainite
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D2211/00Microstructure comprising significant phases
    • C21D2211/005Ferrite
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D2211/00Microstructure comprising significant phases
    • C21D2211/008Martensite

Definitions

  • the present invention relates to a high-strength hot-rolled steel sheet with a low yield ratio excellent in terms of stability of properties after processing has been performed which can preferably be used as a material for a steel pipe for use in, for example, pipelines, oil country tubular goods, and civil engineering and construction, in particular, for a steel pipe of grade X80 specified in the API Standards and to a method for manufacturing the steel sheet.
  • pipelines are constructed in cold areas having, for example, large natural gas reserves in many cases. Therefore, steel sheets as a material for linepipes are required to have excellent low-temperature toughness as well as high strength.
  • linepipes which are laid over a long distance tend to be affected by crustal movement.
  • steel pipes are required to have deformability in the circumferential direction thereof, that is, a stably low yield ratio.
  • Patent Literature 1 proposes a technique for manufacturing a hot-rolled steel sheet including heating a steel slab having a chemical composition containing C: 0.03 wt% to 0.12 wt%, Si: 0.50 wt% or less, Mn: 1.70 wt% or less, P: 0.025 wt% or less, S: 0.025 wt% or less, Al: 0.070 wt% or less, and at least one of Nb: 0.01 wt% to 0.05 wt%, V: 0.01 wt% to 0.02 wt%, and Ti: 0.01 wt% to 0.20 wt% to a temperature of 1180°C to 1300°C, then performing hot rolling with a rough rolling finishing temperature of 950°C to 1050°C and a finish rolling temperature of 760°C to 800°C, performing cooling at a cooling rate of 5°C
  • Patent Literature 1 states that, by using the manufacturing method described above, it is possible to manufacture a hot-rolled steel sheet having a tensile strength of 60 kg/mm 2 or more (590 MPa or more), a low yield ratio of 85% or less, and a low-temperature toughness corresponding to a ductile-brittle transition temperature of -60°C or lower.
  • Patent Literature 2 states that, by manufacturing a hot-rolled steel sheet by using the method described above, it is possible to obtain a hot-rolled steel sheet having a microstructure including bainitic ferrite as a main phase, 3 vol% or more of martensite, and 1 vol% or more of retained austenite as needed, and that, by forming the obtained hot-rolled steel sheet into a pipe, it is possible to manufacture an electric resistance welded steel pipe having a low yield ratio of 85% or less, a low-temperature toughness corresponding to a ductile-brittle transition temperature of -50°C or lower, and excellent plastic-deformation-absorbing capability.
  • Patent Literature 3 states that, by controlling the main phase of a hot-rolled steel sheet to be bainitic ferrite having an average grain diameter of 10 ⁇ m or less, it is possible to achieve a desired high strength after pipe making has been performed and to obtain a hot-rolled steel sheet having excellent low-temperature toughness.
  • Patent Literature 3 states that, by controlling the second phase to be a microstructure including 3.0% or more, in terms of area ratio, of martensite dispersed, it is possible to achieve a low yield ratio.
  • Patent Literature 3 states that, by specifying the chemical composition and microstructure of a hot-rolled steel sheet as described above, it is possible to obtain a high-strength hot-rolled steel sheet with a low yield ratio excellent in terms of low-temperature toughness undergoing only a little decrease in strength after pipe making has been performed and having a yield strength in a direction at 30 degrees from the rolling direction of 480 MPa or more, a ductile-brittle transition temperature vTrs in a Charpy impact test of -80°C or lower, and a low yield ratio of 85% or less.
  • steel having a comparatively good low-temperature toughness has a low strength
  • the steel does not have strength as an X80 grade in the case of, for example, a spiral steel pipe which is subjected to smaller forming strain than an electric resistance welded steel pipe.
  • Patent Literature 3 a decrease in strength after pipe making has been performed is suppressed by controlling a microstructure to be one including martensite, and, optionally, bainite as a second phase.
  • a microstructure to be one including martensite, and, optionally, bainite as a second phase.
  • bainite as a second phase.
  • the degree of work hardening widely varies depending on the amount of forming strain when pipe making is performed.
  • the present invention solves the problems with the conventional techniques described above, and an object of the present invention is to provide a hot-rolled steel sheet which can preferably be used as a material for an X80 grade electric resistance welded steel pipe or a material for an X80 grade spiral steel pipe having a high strength, a high toughness, a low-yield-ratio property, and excellent stability of properties after pipe forming and to provide a method for manufacturing the steel sheet.
  • an object is to provide a hot-rolled steel sheet having a tensile strength of 650 MPa or more, a yield strength of 555 MPa or more, a yield ratio of 90% or less, and a ductile-brittle transition temperature vTrs in a Charpy impact test of -80°C or lower with which it is possible to control a variation in yield ratio ⁇ YR in the circumferential direction of the steel pipe (having a strain t/D x 100 in the circumferential direction of the steel pipe of 1% or more and 9% or less, where D denotes the outer diameter of the steel pipe and t denotes the thickness of the hot-rolled steel sheet before pipe making is performed) of less than 10% after pipe making has been performed, and to provide a method for manufacturing the steel sheet.
  • Patent Literature 3 by controlling the main phase of a hot-rolled steel sheet to be bainitic ferrite having an average grain diameter of 10 ⁇ m or less, it is possible to achieve a desired high strength after pipe making has been performed and to obtain a hot-rolled steel sheet having excellent low-temperature toughness.
  • the second phase of a hot-rolled steel sheet is controlled to be martensite or bainite, and, in particular, in the case of an electric resistance welded steel pipe where the amount of forming strain which is applied to a steel sheet during pipe manufacturing widely varies with location in the circumferential direction of the pipe, yield ratio widely varies with location in the circumferential direction of the steel pipe.
  • the present inventors diligently conducted investigations regarding a second phase with which a low-yield-ratio property is stably realized independently of the amount of forming strain applied after processing has been performed in the case of a hot-rolled steel sheet having a microstructure including bainitic ferrite having an average grain diameter of 10 ⁇ m or less as a main phase.
  • the present inventors focused on the utilization of retained austenite as a second phase with which it is possible to achieve a low yield ratio.
  • Retained austenite which is a soft microstructure, is an advantageous microstructure for controlling the yield ratio of steel to be low.
  • retained austenite since retained austenite gradually transforms into strain-induced martensite starting from a lower C concentration portion, it is possible to keep a yield ratio to be low by increasing tensile strength while keeping yield strength comparatively low.
  • the present inventors conducted investigations regarding the influence of the amount of retained austenite included in a hot-rolled steel sheet as a second phase on a low-yield-ratio property after processing has been performed, and, as a result, found that, in the case where retained austenite is dispersed as a second phase in a hot-rolled steel sheet in an amount of 0.5% or more and 9.5% or less, in terms of volume fraction, it is possible to achieve a low yield ratio of 90% or less when forming strain in a range of 1% to 15% is applied. In addition, it was also found that, as a result of retained austenite transforms into strain-induced martensite, there is an increase in the post-forming tensile strength of a hot-rolled steel sheet.
  • the present inventors conducted additional investigations, and, as a result, found that, by containing retained austenite and martensite as the second phases in a hot-rolled steel sheet, it is possible to control the yield ratio to be almost constant independently of the amount of forming strain.
  • the Bauschinger effect is a phenomenon in which, in the case where a tensile test is performed after plastic deformation in the opposite direction (compressive direction) to the tensile direction has been applied, there is a decrease in yield strength compared with the case without the deformation in the compressive direction. Since the inner surface of a steel pipe is subjected to compressive plastic deformation in the pipe forming process, the Bauschinger effect is expected to be realized. That is, it is considered that, since a decrease in yield strength due to the Bauschinger effect and an increase in yield strength due to the transformation induced plasticity of retained austenite balance each other, a yield ratio is almost constant independently of the amount of forming strain.
  • the present inventors conducted investigations regarding a method for easily manufacturing, without a decrease in production efficiency, a hot-rolled steel sheet having a desired microstructure described above (microstructure including 90% or more, in terms of volume fraction, of bainitic ferrite having an average grain diameter of 10 ⁇ m or less as a main phase and 0.5% or more and 9.5% or less, in terms of volume fraction, of retained austenite and 0.5% or more and 9.5% or less, in terms of volume fraction, of martensite as second phases), and, as a result, found that it is possible to manufacture a hot-rolled steel sheet having a desired microstructure with a high efficiency and ease without performing a special process such as air cooling in a cooling process before a coiling process following a hot rolling process by performing hot-rolling on a continuously cast slab having a specified chemical composition with, for example, specified slab heating conditions, finish rolling conditions, cooling rate in the central portion in the thickness direction of the steel sheet in a cooling process following finish rolling, and the weight and width of a coil.
  • a special process
  • a hot-rolled steel sheet having a high strength, a high toughness, and a low-yield-ratio property excellent in terms of stability of properties after processing has been performed which can preferably be used as a material for a steel pipe for use in, for example, pipelines, oil country tubular goods, and civil engineering and construction, in particular, for a steel pipe of grade X80 specified in the API Standards by using conventional hot rolling equipment, which has a marked effect on the industry.
  • C is a chemical element which is important for achieving the strength (tensile strength and yield strength) of a hot-rolled steel sheet by forming carbides with Nb, V, and Ti and which is indispensable for forming second phases (retained austenite and martensite) important for controlling the yield ratio of a hot-rolled steel sheet to be low.
  • the C content be 0.030% or more.
  • the C content is more than 0.120%, there is a decrease in the toughness of the hot-rolled steel sheet due to an excessive increase in the amount of carbides.
  • the C content is set to be 0.030% or more and 0.120% or less, or preferably 0.040% or more and 0.090% or less.
  • Si 0.05% or more and 0.50% or less
  • the upper limit of the Si content is set to be 0.50%.
  • the lower limit of the Si content is set to be 0.05% in order to achieve the strength of grade X80 through solid solution strengthening.
  • the Si content be 0.10% or more and 0.35% or less.
  • Mn 1.00% or more and 2.20% or less
  • Mn is a chemical element which is necessary for achieving the strength and the toughness of a hot-rolled steel sheet by inhibiting the formation of polygonal ferrite. Also, Mn is a chemical element which is necessary for achieving the low-yield-ratio property of a hot-rolled steel sheet by promoting the formation of second phases and by stably forming retained austenite and martensite. In order to realize such effects, it is necessary that the Mn content be 1.00% or more. On the other hand, in the case where the Mn content is more than 2.20%, there is a tendency for a variation in the mechanical properties of a hot-rolled steel sheet to occur due to center segregation and there is a decrease in toughness.
  • the Mn content is set to be 1.00% or more and 2.20% or less, or preferably 1.40% or more and 2.00% or less.
  • the upper limit of the P content is set to be 0.025%, or preferably 0.018%.
  • the upper limit of the S content is set to be 0.0050%, and the upper limit of the N content is set to be 0.0060%. It is preferable that the S content be 0.0030% or less and that the N content be 0.0040% or less.
  • the lower limits of the contents of P, S, and N are all decided in consideration of the practical limit of the control capability of a steel making process, it is preferable that the lower limits of each of the P content and the N content be 0.0010% and that the lower limit of the S content be 0.0001%.
  • Al 0.005% or more and 0.100% or less
  • Al is effective as a deoxidizing agent for steel, and the Al content is set to be 0.005% or more with which the effect of deoxidizing is realized.
  • the Al content is set to be 0.005% or more and 0.100% or less, or preferably 0.010% or more and 0.050% or less.
  • Nb 0.020% or more and 0.100% or less
  • Nb is effective for decreasing a grain diameter and is a precipitation strengthening chemical element, and it is necessary that the Nb content be 0.020% or more in order to achieve a steel pipe strength of grade X80.
  • the Nb content is set to be 0.020% or more and 0.100% or less, or preferably 0.030% or more and 0.080% or less.
  • Mo is a chemical element which is effective for increasing the strength of a hot-rolled steel sheet by inhibiting austenite in a steel sheet from transforming into polygonal ferrite or pearlite in a cooling process following a hot rolling process when a hot-rolled steel sheet is manufactured.
  • Mo is a chemical element which is necessary to achieve a satisfactory low-yield-ratio property of a hot-rolled steel sheet by promoting the formation of second phases (retained austenite and martensite). In order to realize such effects, the Mo content is set to be 0.05% or more.
  • the Mo content is set to be 0.05% or more and 0.50% or less, or preferably 0.10% or more and 0.35% or less.
  • Ti is a chemical element which is effective for decreasing a grain diameter and a precipitation strengthening chemical element, and it is necessary that the Ti content be 0.001% or more in order to realize such effects.
  • the Ti content is set to be 0.001% or more and 0.100% or less, or preferably 0.010% or more and 0.040% or less.
  • Cr is a chemical element which is effective for delaying pearlite transformation in a cooling process following a hot rolling process when a hot-rolled steel sheet is manufactured and which is effective for decreasing the amount of intergranular cementite.
  • Cr is a chemical element which is necessary to achieve the low-yield-ratio property of a hot-rolled steel sheet by promoting the formation of retained austenite and martensite, which are second phases.
  • the Cr content is set to be 0.05% or more.
  • the Cr content is more than 0.50%, there is a decrease in the toughness of a hot-rolled steel sheet due to the formation of excessive amounts of retained austenite and martensite, which are second phases.
  • the Cr content is set to be 0.05% or more and 0.50% or less, or preferably 0.10% or more and 0.35% or less.
  • the Ca content is set to be 0.0005% or more.
  • the Ca content is set to be 0.0050% or less. It is preferable that the Ca content be 0.0010% or more and 0.0030% or less.
  • the chemical composition described above is the basic chemical composition of a hot-rolled steel sheet according to the present invention
  • one, two, or more selected from among V: 0.001% or more and 0.100% or less, Cu: 0.001% or more and 0.50% or less, Ni: 0.001% or more and 1.00% or less, and B: 0.0040% or less may be added in addition to the basic chemical composition described above.
  • V 0.001% or more and 0.100% or less
  • V is a precipitation strengthening chemical element, and it is preferable that the V content be 0.001% or more in order to realize such an effect.
  • the V content in the case where the V content is excessively large, since an excessive amount of precipitates is formed in the coiling temperature range (400°C or higher and 650°C or lower) described below when a hot-rolled steel sheet is manufactured, there may be a decrease in toughness and elongation property, and there may be a decrease in weldability. Therefore, it is preferable that the V content be 0.001% or more and 0.100% or less, or more preferably 0.020% or more and 0.080% or less.
  • Cu 0.001% or more and 0.50% or less
  • Cu is a chemical element which is effective for inhibiting austenite in a steel sheet from transforming into polygonal ferrite or pearlite in a cooling process following a hot rolling process when a hot-rolled steel sheet is manufactured and which is effective for increasing the strength of a hot-rolled steel sheet.
  • the Cu content be 0.001% or more.
  • the Cu content be 0.001% or more and 0.50% or less, or more preferably 0.10% or more and 0.40% or less.
  • Ni 0.001% or more and 1.00% or less
  • Ni is a chemical element which is effective for inhibiting austenite in a steel sheet from transforming into polygonal ferrite or pearlite in a cooling process following a hot rolling process when a hot-rolled steel sheet is manufactured and which is effective for increasing the strength of a hot-rolled steel sheet.
  • the Ni content be 0.001% or more.
  • the Ni content be 0.001% or more and 1.00% or less, or more preferably 0.10% or more and 0.50% or less.
  • the B is effective for preventing the formation of polygonal ferrite by inhibiting ferrite transformation at a high temperature in a cooling process following finish rolling when a hot-rolled steel sheet is manufactured.
  • the B content be 0.0001% or more.
  • the B content be 0.0040% or less, or more preferably 0.0002% or more and 0.0010% or less.
  • constituent chemical elements other than those described above are Fe and inevitable impurities.
  • the inevitable impurities include Co, W, Pb, and Sn, and it is preferable that the content of each of these chemical elements be 0.02% or less.
  • the hot-rolled steel sheet according to the present invention has a microstructure including bainitic ferrite as a main phase and martensite and retained austenite as second phases, in which the volume fraction of the main phase is 90% or more, in which the average grain diameter of the main phase is 10 ⁇ m or less, in which the volume fraction of the martensite is 0.5% or more and 9.5% or less, and in which the volume fraction of the retained austenite is 0.5% or more and 9.5% or less.
  • bainitic ferrite is a microstructure including a substructure having a high dislocation density in which cementite is not precipitated in grains.
  • bainite is different from bainitic ferrite in that bainite includes a lath structure having a high dislocation density in which cementite is precipitated in grains.
  • polygonal ferrite is different from bainitic ferrite in that polygonal ferrite has a very low dislocation density.
  • Average grain diameter of bainitic ferrite 10 ⁇ m or less
  • the hot-rolled steel sheet by controlling the main phase of a hot-rolled steel sheet to be a fine bainitic ferrite excellent in terms of strength-toughness balance, the hot-rolled steel sheet is provided with a desired strength and low-temperature toughness.
  • the volume fraction of bainitic ferrite, which is a main phase to be 90% or more, and by controlling the average grain diameter of the bainitic ferrite to be 10 ⁇ m or less, it is possible to achieve satisfactory strength and low-temperature toughness of a hot-rolled steel sheet through the effect of a decrease in grain diameter.
  • the volume fraction of bainitic ferrite be 91% or more, and it is preferable that the average grain diameter of bainitic ferrite be 3.0 ⁇ m or less.
  • the average grain diameter of bainitic ferrite be 3.0 ⁇ m or less in the case where the total volume fraction of martensite and retained austenite is 4.0% or more.
  • the volume fraction of bainitic ferrite since there is a significant decrease in the volume fraction of second phases (retained austenite and martensite), which are important for decreasing the yield ratio of a hot-rolled steel sheet, in the case where the volume fraction of bainitic ferrite is excessively large, it is preferable that the volume fraction of bainitic ferrite be 95% or less.
  • the grain diameter of bainitic ferrite be as small as possible, the lower limit of the average grain diameter thereof is substantially about 1 ⁇ m.
  • volume fraction of retained austenite 0.5% or more and 9.5% or less
  • the volume fraction of retained austenite be 0.5% or more, or preferably 2.0% or more.
  • the volume fraction of retained austenite is more than 9.5%, since retained austenite functions as a crack propagation path, there is a decrease in the low-temperature toughness of a hot-rolled steel sheet. Therefore, it is necessary that the volume fraction of retained austenite be 9.5% or less.
  • the volume fraction of retained austenite be 5% or less in order to achieve further increased low-temperature toughness.
  • volume fraction of martensite 0.5% or more and 9.5% or less
  • Martensite increases the Bauschinger effect by facilitating the formation of movable dislocations during processing into bainitic ferrite.
  • the volume fraction of martensite be 0.5% or more, or preferably 2.5% or more.
  • the volume fraction of martensite be 9.5% or less.
  • the volume fraction of martensite be 5% or less in order to achieve further increased low-temperature toughness.
  • the microstructure of the hot-rolled steel sheet according to the present invention may include pearlite and cementite in addition to bainitic ferrite, retained austenite, and martensite described above. It is preferable that the volume fraction of the microstructures other than bainitic ferrite, retained austenite, and martensite, that is, pearlite and cementite be limited to 2% or less in total. In addition, it is preferable that the thickness of the hot-rolled steel sheet according to the present invention to be used as a material mainly for a linepipe be 15 mm or more and 30 mm or less.
  • the hot-rolled steel sheet according to the present invention by cooling a slab (cast piece) having the chemical composition described above which has been obtained by using a continuous casting method to a specified temperature or less, by then heating the cooled slab, by then performing rough rolling and finish rolling on the heated slab, by then performing accelerated cooling on the rolled steel sheet under specified conditions, and by then coiling the cooled steel sheet at a specified temperature in order to obtain a coil having a specified weight and width.
  • Cooling temperature of a continuously cast slab 600°C or lower
  • a continuously cast slab which has not undergone ferrite transformation has an austenite structure and has a very large grain diameter because it has been exposed to a high temperature for a long time. Therefore, such a large austenite grain diameter is decreased through ferrite transformation. Therefore, the continuously cast slab is cooled to a temperature of 600°C or lower, or preferably 500°C or lower, at which ferrite transformation is almost completed. Here, subsequently, the continuously cast slab is heated so as to undergo reverse transformation into austenite, which results in a further decrease in grain diameter.
  • Heating temperature of a continuously cast slab 1050°C or higher and 1300°C or lower
  • the reheating temperature of a continuously cast slab is set to be 1050°C or higher and 1300°C or lower, or preferably 1150°C or higher and 1230°C or lower.
  • the heated slab (continuously cast piece) is subjected to rough rolling and finish rolling so as to have an arbitrary thickness, and there is no particular limitation on what condition is used for rough rolling in the present invention.
  • Rolling reduction in the non-recrystallization temperature range when finish rolling is performed 20% or more and 85% or less
  • the rolling reduction described above is set to be 20% or more and 85% or less, or preferably 35% or more and 75% or less.
  • Finishing delivery temperature equal to or higher than (Ar 3 - 50°C) and equal to or lower than (Ar 3 + 100°C)
  • the finishing delivery temperature be equal to or higher than (Ar 3 - 50°C).
  • the finishing delivery temperature is lower than (Ar 3 - 50°C)
  • Polygonal ferrite has a larger grain diameter than that of bainitic ferrite which is formed during a subsequent cooling process or after the cooling has been performed, which results in the formation of a mixed grain structure having a variation in grain diameter. Therefore, it is not possible to achieve desired properties of a hot rolled steel sheet.
  • the finishing delivery temperature is higher than (Ar 3 + 100°C), since there is an increase in bainitic ferrite grain diameter, there is a decrease in the toughness of a hot-rolled steel sheet.
  • the finishing delivery temperature is set to be equal to or higher than (Ar 3 - 50°C) and equal to or lower than (Ar 3 + 100°C), or preferably equal to or higher than (Ar 3 - 20°C) and equal to or lower than (Ar 3 + 50°C).
  • finishing delivery temperature refers to the surface temperature of a steel sheet determined at the exit of a finish rolling mill.
  • accelerated cooling is performed under the following conditions. It is preferable that accelerated cooling be started within 7 seconds, or more preferably within 3 seconds, after finish rolling has been performed. In the case where the time until accelerated cooling is started after finish rolling has been performed is more than 7 seconds, there may be an increase in grain diameter, or ferrite transformation may start so that polygonal ferrite is formed.
  • an average cooling rate at the central position in the thickness direction of the steel sheet in a temperature range from the cooling start temperature to 650°C be 10°C/s or more.
  • the cooling rate at the central position in the thickness direction of the steel sheet in the temperature range described above is excessively high, since there is an increase in the surface hardness of the steel sheet, the steel sheet is unsuitable for a steel sheet for a linepipe. Therefore, it is necessary that the upper limit of the average cooling rate described above be 100°C/s. It is preferable that the average cooling rate be 25°C/s or more and 50°C/s or less.
  • Cooling stop temperature at the central position in the thickness direction of the steel sheet 420°C or higher and 650°C or lower
  • the temperature at which accelerated cooling is stopped be 420°C or higher in terms of the temperature at the central position in the thickness direction of the steel sheet.
  • the cooling stop temperature of accelerated cooling be 420°C or higher and 650°C or lower, or preferably 500°C or higher and 590°C or lower, in terms of the temperature at the central position in the thickness direction of the steel sheet.
  • Coiling temperature 400°C or higher and 650°C or lower
  • austenite and martensite which are second phases, are formed in an air cooling process following a coiling process. Therefore, it is necessary that C be diffused from bainitic ferrite, which is formed through transformation in the accelerated cooling process or after cooling has been stopped, to untransformed austenite.
  • C is diffused from bainitic ferrite to untransformed austenite
  • since C is concentrated in the untransformed austenite the untransformed austenite is inhibited from transforming into bainite, which results in martensite or retained austenite (untransformed austenite cooled to room temperature with the microstructure being unchanged) being obtained from the untransformed austenite.
  • martensite or retained austenite is obtained depends on the degree of the C concentration, and retained austenite is obtained in a portion in which there is an increase in C concentration so that the Ms point (temperature at which martensite transformation starts) is lower than room temperature.
  • the coiling temperature be 400°C or higher.
  • the coiling temperature is higher than 650°C, since polygonal ferrite and pearlite having a large grain diameter are formed, it is not possible to achieve a desired microstructure of a hot-rolled steel sheet. Therefore, it is necessary that the coiling temperature be 400°C or higher and 650°C or lower, or preferably 480°C or higher and 580°C or lower.
  • the "coiling temperature” described above refers to the temperature at the central position in the thickness direction of the steel sheet in any case.
  • Coil weight after coiling has been performed: 20 tons or more
  • Coil width after coiling has been performed: 1000 mm or more
  • the coil weight be 20 tons or more and the coil width be 1000 mm or more.
  • the coil weight after coiling has been performed is less than 20 tons or the coil width after coiling has been performed is less than 1000 mm, since the amount of C concentrated is not sufficient for austenite retained in the untransformed state to be stable due to excessive large air cooling rate after coiling has been performed, only martensite is preferentially formed as a second phase.
  • the air cooling rate after coiling has been performed be 70°C/s or less, or more preferably 50°C/s or less.
  • the "air cooling rate after coiling has been performed” refers to an average cooling rate in a temperature range of 400°C to 390°C in terms of the temperature of a steel sheet. The temperature of a coil is determined at the central position in the width direction of the peripheral surface of the coil after coiling has been performed.
  • the temperature of a coil is determined by using a thermocouple that is attached to a proper portion of the steel sheet where the steel sheet is coiled tightly such that no air gap is formed therein, the portion being positioned at the center in the width direction of the peripheral surface of the steel sheet.
  • the reason for defining an air cooling rate after coiling has been performed as an average cooling rate in a temperature range of 400°C to 390°C is because C is most likely to be concentrated in austenite retained in the untransformed state in a temperature range around 400°C.
  • the coil weight after coiling has been performed is set to be 20 tons or more and the coil width after coiling has been performed is set to be 1000 mm or more.
  • the coil weight after coiling has been performed be 25 tons or more and the coil width after coiling has been performed be 1400 mm or more.
  • the substantial upper limits of the coil weight and coil width are respectively about 40 tons and about 2500 mm.
  • Ar 3 points given in Table 2 were determined from thermal expansion curves obtained by taking samples for thermal expansion determination from the obtained slabs, by transforming them into austenite at a temperature of 950°C, and by then cooling the samples at a cooling rate of 5°C/min.
  • microstructure observation By taking test pieces from the obtained hot-rolled steel sheets and the electric resistance welded steel pipes, microstructure observation, a tensile test, and a Charpy impact test were performed.
  • the methods for microstructure observation and the various tests were as follows.
  • the volume fraction of bainitic ferrite was defined as the average value of the area ratios determined at all of the positions in the thickness direction described above.
  • the volume fraction of pearlite was defined as the average value of the area ratios determined at all of the positions in the thickness direction described above.
  • the volume fraction of polygonal ferrite was determined.
  • the average grain diameter of bainitic ferrite was defined as the circle-equivalent diameter obtained by performing image analysis on the microstructures which were recognized as bainitic ferrite.
  • the total volume fraction of retained austenite and martensite was defined as the average value of the area ratios determined at all of the positions in the thickness direction described above.
  • the volume fraction of martensite was defined as the result of subtracting the volume fraction of retained austenite from the total volume fraction described above.
  • volume fraction of retained austenite was determined by using the X-ray diffraction method described below.
  • a V-notch test piece (having a length of 55 mm, a height of 10 mm, and a width of 10 mm) from the central position in the thickness direction of the obtained hot-rolled steel sheet so that the longitudinal direction of the test piece was a direction (C-direction) at a right angle to the rolling direction, and by performing a Charpy impact test in accordance with the prescription in JIS Z 2242, a ductile-brittle transition temperature (°C) was determined.
  • three test pieces were taken from each of the hot-rolled steel sheets, and the ductile-brittle transition temperature (vTrs) of each of the hot-rolled steel sheet was defined as the arithmetic average value of the obtained ductile-brittle transition temperatures of the three test pieces.
  • the hot-rolled steel sheets of the examples of the present invention were good in terms of all of tensile properties (yield strength, tensile strength, yield ratio, and the difference in yield ratio of an electric resistance welded steel pipe) and toughness (low-temperature toughness).
  • the hot-rolled steel sheets of the comparative examples were unsatisfactory in terms of one or both of tensile properties and toughness (low-temperature toughness).

Description

    Technical Field
  • The present invention relates to a high-strength hot-rolled steel sheet with a low yield ratio excellent in terms of stability of properties after processing has been performed which can preferably be used as a material for a steel pipe for use in, for example, pipelines, oil country tubular goods, and civil engineering and construction, in particular, for a steel pipe of grade X80 specified in the API Standards and to a method for manufacturing the steel sheet.
  • Background Art
  • With the globally growing trend away from nuclear power generation, it is expected that there will be a further growing demand for fossil energy in the future. Accordingly, it is assumed that there will be a growing demand for high-strength linepipes having a large diameter and a thick wall in order to increase transportation efficiency of natural gases and oils. To date, UOE steel pipes, which are manufactured from thick steel plates, have been mainly used as linepipes for high-pressure operation. Nowadays, however, since there is a strong demand for decreasing the material costs of steel pipes, for example, in order to decrease the construction costs of pipelines and due to the insufficient supply capacity of UOE steel pipes, there is a trend toward using electric resistance welded steel pipes and spiral steel pipes, which are manufactured from hot-rolled steel sheets with higher productivity and lower cost than UOE steel pipes.
  • Here, pipelines are constructed in cold areas having, for example, large natural gas reserves in many cases. Therefore, steel sheets as a material for linepipes are required to have excellent low-temperature toughness as well as high strength. In addition, linepipes which are laid over a long distance tend to be affected by crustal movement. In order to prevent pipes from bursting due to pressure fluctuations therein when a pipeline fractures and the leakage of the transported gas occurs by some chance due to forced deformation caused by crustal movement, steel pipes are required to have deformability in the circumferential direction thereof, that is, a stably low yield ratio.
  • In such a situation, various techniques regarding a hot-rolled steel sheet as a material for a linepipe have been proposed. For example, Patent Literature 1 proposes a technique for manufacturing a hot-rolled steel sheet including heating a steel slab having a chemical composition containing C: 0.03 wt% to 0.12 wt%, Si: 0.50 wt% or less, Mn: 1.70 wt% or less, P: 0.025 wt% or less, S: 0.025 wt% or less, Al: 0.070 wt% or less, and at least one of Nb: 0.01 wt% to 0.05 wt%, V: 0.01 wt% to 0.02 wt%, and Ti: 0.01 wt% to 0.20 wt% to a temperature of 1180°C to 1300°C, then performing hot rolling with a rough rolling finishing temperature of 950°C to 1050°C and a finish rolling temperature of 760°C to 800°C, performing cooling at a cooling rate of 5°C/s to 20°C/s, starting air cooling at a temperature higher than 670°C, continuing air cooling for 5 seconds to 20 seconds, then performing cooling at a cooling rate of 20°C/s or more, and performing coiling at a temperature of 500°C or lower. In addition, Patent Literature 1 states that, by using the manufacturing method described above, it is possible to manufacture a hot-rolled steel sheet having a tensile strength of 60 kg/mm2 or more (590 MPa or more), a low yield ratio of 85% or less, and a low-temperature toughness corresponding to a ductile-brittle transition temperature of -60°C or lower.
  • In addition, Patent Literature 2 proposes a technique including hot-rolling a slab having a chemical composition containing, by mass%, C: 0.01% to 0.09%, Si: 0.50% or less, Mn: 2.5% or less, Al: 0.01% to 0.10%, Nb: 0.005% to 0.10%, and one, two, or more of Mo: 0.5% or less, Cu: 0.5% or less, Ni: 0.5% or less, Cr: 0.5% or less, in which Mneq (Mneq (%) = Mn + 0.26Si + 3.5P + 1.30Cr + 0.37Ni + 2.67Mo), which is a relational expression of the contents of Mn, Si, P, Cr, Ni, and Mo, satisfies 2.0 or more, cooling the hot-rolled steel sheet to a temperature of 500°C to 650°C at a cooling rate of 5°C/s or more, coiling the cooled steel sheet, holding the coiled steel sheet in this temperature range for 10 minutes or more, then cooling the held steel sheet to a temperature lower than 500°C in order to obtain a hot-rolled steel sheet, and forming the obtained hot-rolled steel sheet into a pipe in order to obtain an electric resistance welded steel pipe. In addition, Patent Literature 2 states that, by manufacturing a hot-rolled steel sheet by using the method described above, it is possible to obtain a hot-rolled steel sheet having a microstructure including bainitic ferrite as a main phase, 3 vol% or more of martensite, and 1 vol% or more of retained austenite as needed, and that, by forming the obtained hot-rolled steel sheet into a pipe, it is possible to manufacture an electric resistance welded steel pipe having a low yield ratio of 85% or less, a low-temperature toughness corresponding to a ductile-brittle transition temperature of -50°C or lower, and excellent plastic-deformation-absorbing capability.
  • In addition, Patent Literature 3 proposes a technique which includes controlling the chemical composition of a hot-rolled steel sheet to be one containing, by mass%, C: 0.03% to 0.11%, Si: 0.01% to 0.50%, Mn: 1.0% to 2.2%, P: 0.025% or less, S: 0.005% or less, Al: 0.005% to 0.10%, Nb: 0.01% to 0.10%, Ti: 0.001% to 0.05%, B: 0.0005% or less, one, two, or all of Cr: 0.01% to 1.0%, Mo: 0.01% to 0.5%, and Ni: 0.01% to 0.5%, and the balance being Fe and inevitable impurities, in which Mneq (Mneq (%) = Mn + 0.26Si + 1.30Cr + 2.67Mo + 0.8Ni), which is a relational expression of the contents of Mn, Si, Cr, Mo, and Ni, falls within a range of 2.0% to 4.0%, and controlling the microstructure of the hot-rolled steel sheet to be one including bainitic ferrite as a main phase, and at least 3.0%, in terms of area ratio, of martensite as a second phase, in which the average grain diameter of the bainitic ferrite is 10 µm or less. In addition, Patent Literature 3 states that, by controlling the main phase of a hot-rolled steel sheet to be bainitic ferrite having an average grain diameter of 10 µm or less, it is possible to achieve a desired high strength after pipe making has been performed and to obtain a hot-rolled steel sheet having excellent low-temperature toughness. In addition, Patent Literature 3 states that, by controlling the second phase to be a microstructure including 3.0% or more, in terms of area ratio, of martensite dispersed, it is possible to achieve a low yield ratio. Moreover, Patent Literature 3 states that, by specifying the chemical composition and microstructure of a hot-rolled steel sheet as described above, it is possible to obtain a high-strength hot-rolled steel sheet with a low yield ratio excellent in terms of low-temperature toughness undergoing only a little decrease in strength after pipe making has been performed and having a yield strength in a direction at 30 degrees from the rolling direction of 480 MPa or more, a ductile-brittle transition temperature vTrs in a Charpy impact test of -80°C or lower, and a low yield ratio of 85% or less.
  • Citation List Patent Literature
    • PTL 1: Japanese Unexamined Patent Application Publication No. 63-227715
    • PTL 2: Japanese Unexamined Patent Application Publication No. 2006-299413
    • PTL 3: Japanese Unexamined Patent Application Publication No. 2012-172256
    Summary of Invention Technical Problem
  • However, in the case of all of the conventional techniques described above, it is very difficult to obtain a hot-rolled steel sheet which can preferably be used as a material for an X80 grade linepipe. That is, it is very difficult to obtain a thick hot-rolled steel sheet having a high strength, excellent low-temperature toughness, a sufficient low-yield-ratio property which is effective against forced deformation caused by, for example, intense processing conditions when pipe making is performed or crustal movement after a pipeline has been constructed, and excellent stability of properties after processing has been performed (after pipe making has been performed).
  • In the case of the technique proposed by Patent Literature 1, there is a problem in that the hot-rolled steel sheet does not have strength as an X80 grade and in that there is a significant decrease in production efficiency because, for example, an air cooling process is included in a cooling process. In the case of the technique proposed by Patent Literature 2, it is not possible to stably achieve a ductile-brittle transition temperature vTrs of -80°C or lower, which is required for a cold-area-specification material having a good low-temperature toughness for which there is a growing demand nowadays. In addition, since steel having a comparatively good low-temperature toughness has a low strength, there may be a case where the steel does not have strength as an X80 grade in the case of, for example, a spiral steel pipe which is subjected to smaller forming strain than an electric resistance welded steel pipe.
  • In the case of the technique proposed by Patent Literature 3, a decrease in strength after pipe making has been performed is suppressed by controlling a microstructure to be one including martensite, and, optionally, bainite as a second phase. However, in the case where only martensite or bainite is dispersed as a second phase, the degree of work hardening widely varies depending on the amount of forming strain when pipe making is performed. Therefore, for example, in the case of an electric resistance welded steel pipe where there is usually a difference in the amount of forming strain between a position located at 90 degrees and a position located at 180 degrees (in the circumferential direction from the welded part which is assumed to be located at 0 degrees), there is a problem in that properties, in particular, a yield ratio varies with location in the circumferential direction of the pipe. In the case where a yield ratio varies in the circumferential direction of the pipe as described above, there may be a problem in that the steel pipe undergoes buckling deformation because deformation is concentrated in a portion having a low yield ratio (low yield strength) when the steel pipe is deformed by being subjected to an external force caused by, for example, a crustal movement such as land subsidence or earthquake. Once a steel pipe undergoes buckling, since deformation is concentrated in the portion where buckling has occurred, the steel pipe tends to fracture because this portion further deforms.
  • The present invention solves the problems with the conventional techniques described above, and an object of the present invention is to provide a hot-rolled steel sheet which can preferably be used as a material for an X80 grade electric resistance welded steel pipe or a material for an X80 grade spiral steel pipe having a high strength, a high toughness, a low-yield-ratio property, and excellent stability of properties after pipe forming and to provide a method for manufacturing the steel sheet. Specifically, an object is to provide a hot-rolled steel sheet having a tensile strength of 650 MPa or more, a yield strength of 555 MPa or more, a yield ratio of 90% or less, and a ductile-brittle transition temperature vTrs in a Charpy impact test of -80°C or lower with which it is possible to control a variation in yield ratio ΔYR in the circumferential direction of the steel pipe (having a strain t/D x 100 in the circumferential direction of the steel pipe of 1% or more and 9% or less, where D denotes the outer diameter of the steel pipe and t denotes the thickness of the hot-rolled steel sheet before pipe making is performed) of less than 10% after pipe making has been performed, and to provide a method for manufacturing the steel sheet.
  • Solution to Problem
  • As described in Patent Literature 3, by controlling the main phase of a hot-rolled steel sheet to be bainitic ferrite having an average grain diameter of 10 µm or less, it is possible to achieve a desired high strength after pipe making has been performed and to obtain a hot-rolled steel sheet having excellent low-temperature toughness. However, in the case of the technique proposed in Patent Literature 3 where the second phase of a hot-rolled steel sheet is controlled to be martensite or bainite, and, in particular, in the case of an electric resistance welded steel pipe where the amount of forming strain which is applied to a steel sheet during pipe manufacturing widely varies with location in the circumferential direction of the pipe, yield ratio widely varies with location in the circumferential direction of the steel pipe. In order to solve such a problem, the present inventors diligently conducted investigations regarding a second phase with which a low-yield-ratio property is stably realized independently of the amount of forming strain applied after processing has been performed in the case of a hot-rolled steel sheet having a microstructure including bainitic ferrite having an average grain diameter of 10 µm or less as a main phase.
  • First, the present inventors focused on the utilization of retained austenite as a second phase with which it is possible to achieve a low yield ratio. Retained austenite, which is a soft microstructure, is an advantageous microstructure for controlling the yield ratio of steel to be low. In addition, in the case where forming strain is applied to a hot-rolled steel sheet having a microstructure including retained austenite as a second phase, since retained austenite gradually transforms into strain-induced martensite starting from a lower C concentration portion, it is possible to keep a yield ratio to be low by increasing tensile strength while keeping yield strength comparatively low.
  • Therefore, the present inventors conducted investigations regarding the influence of the amount of retained austenite included in a hot-rolled steel sheet as a second phase on a low-yield-ratio property after processing has been performed, and, as a result, found that, in the case where retained austenite is dispersed as a second phase in a hot-rolled steel sheet in an amount of 0.5% or more and 9.5% or less, in terms of volume fraction, it is possible to achieve a low yield ratio of 90% or less when forming strain in a range of 1% to 15% is applied. In addition, it was also found that, as a result of retained austenite transforms into strain-induced martensite, there is an increase in the post-forming tensile strength of a hot-rolled steel sheet.
  • At the same time, however, it was also found that, in the case where the second phase of a hot-rolled steel sheet is composed only of retained austenite, it is not possible to control the post-forming yield ratio of the hot-rolled steel sheet to be constant independently of the amount of forming strain. Therefore, the present inventors conducted additional investigations, and, as a result, found that, by containing retained austenite and martensite as the second phases in a hot-rolled steel sheet, it is possible to control the yield ratio to be almost constant independently of the amount of forming strain. In addition, it was found that, by containing, in terms of volume fraction, 0.5% or more and 9.5% or less of retained austenite and 0.5% or more and 9.5% or less of martensite in combination as second phases, it is possible to stably achieve a low yield ratio in a low- to high-forming-strain range. Although there are many unclear points about the reason why it is possible to control a yield ratio to be almost constant independently of the amount of forming strain by containing retained austenite and martensite, it is thought to be because, by dispersing hard martensite in bainitic ferrite, the Bauschinger effect increases as a result of many movable dislocations generating in bainitic ferrite during pipe forming. The Bauschinger effect is a phenomenon in which, in the case where a tensile test is performed after plastic deformation in the opposite direction (compressive direction) to the tensile direction has been applied, there is a decrease in yield strength compared with the case without the deformation in the compressive direction. Since the inner surface of a steel pipe is subjected to compressive plastic deformation in the pipe forming process, the Bauschinger effect is expected to be realized. That is, it is considered that, since a decrease in yield strength due to the Bauschinger effect and an increase in yield strength due to the transformation induced plasticity of retained austenite balance each other, a yield ratio is almost constant independently of the amount of forming strain. In addition, it was clarified that, by utilizing this knowledge, in particular, even in the case of a steel pipe where the amount of forming strain is large, that is, a steel pipe having a large ratio (the thickness of a hot-rolled steel sheet before pipe manufacturing)/(the outer diameter of the steel pipe) or an electric resistance welded steel pipe, it is possible to stably achieve a low-yield-ratio property.
  • Moreover, the present inventors conducted investigations regarding a method for easily manufacturing, without a decrease in production efficiency, a hot-rolled steel sheet having a desired microstructure described above (microstructure including 90% or more, in terms of volume fraction, of bainitic ferrite having an average grain diameter of 10 µm or less as a main phase and 0.5% or more and 9.5% or less, in terms of volume fraction, of retained austenite and 0.5% or more and 9.5% or less, in terms of volume fraction, of martensite as second phases), and, as a result, found that it is possible to manufacture a hot-rolled steel sheet having a desired microstructure with a high efficiency and ease without performing a special process such as air cooling in a cooling process before a coiling process following a hot rolling process by performing hot-rolling on a continuously cast slab having a specified chemical composition with, for example, specified slab heating conditions, finish rolling conditions, cooling rate in the central portion in the thickness direction of the steel sheet in a cooling process following finish rolling, and the weight and width of a coil.
  • The present invention has been completed on the basis of the findings described above, and the subjective matter of the present invention is as follows.
    1. [1] A hot-rolled steel sheet having a chemical composition consisting of, by mass%, C: 0.030% or more and 0.120% or less, Si: 0.05% or more and 0.50% or less, Mn: 1.00% or more and 2.20% or less, P: 0.025% or less, S: 0.0050% or less, N: 0.0060% or less, Al: 0.005% or more and 0.100% or less, Nb: 0.020% or more and 0.100% or less, Mo: 0.05% or more and 0.50% or less, Ti: 0.001% or more and 0.100% or less, Cr: 0.05% or more and 0.50% or less, Ca: 0.0005% or more and 0.0050% or less, optionally one or more selected from among V: 0.001% or more and 0.100% or less, Cu: 0.001% or more and 0.50% or less, Ni: 0.001% or more and 1.00% or less, and B: 0.0040% or less, and the balance being Fe and inevitable impurities, and having a microstructure including, bainitic ferrite as a main phase and martensite and retained austenite as second phases, in which the volume fraction of the main phase is 90% or more, the average grain diameter of the main phase is 10 µm or less, the volume fraction of the martensite is 0.5% or more and 9.5% or less, and the volume fraction of the retained austenite is 0.5% or more and 9.5% or less, in which a yield ratio of 90% or less, a yield strength of 555 MPa or more, and a tensile strength of 650 MPa or more.
    2. [2] The hot-rolled steel sheet according to item [1] above, the steel sheet having the chemical composition containing, by mass%, one or more selected from among V: 0.001% or more and 0.100% or less, Cu: 0.001% or more and 0.50% or less, Ni: 0.001% or more and 1.00% or less, and B: 0.0040% or less.
    3. [3] A method for manufacturing a hot-rolled steel sheet, the method including: cooling a continuously cast slab having the chemical composition according to item [1] or [2] above to a temperature of 600°C or lower; then heating the cooled slab in a temperature range of 1050°C or higher and 1300°C or lower; performing rough rolling; performing finish rolling following the rough rolling, in which rolling reduction in a non-recrystallization temperature range is 20% or more and 85% or less, and in which a finishing delivery temperature is equal to or higher than (Ar3 - 50°C) and equal to or lower than (Ar3 + 100°C) ; performing cooling following the finish rolling, in which an average cooling rate at the central position in the thickness direction of the steel sheet is 10°C/s or more and 100°C/s or less in a temperature range from the cooling start temperature to 650°C, and in which a cooling stop temperature is 420°C or higher and 650°C or lower; and performing coiling in a temperature range of 400°C or higher and 650°C or lower in order to obtain a coil having a weight of 20 tons or more and a width of 1000 mm or more.
    Advantageous Effects of Invention
  • According to the present invention, it is possible to obtain a hot-rolled steel sheet having a high strength, a high toughness, and a low-yield-ratio property excellent in terms of stability of properties after processing has been performed which can preferably be used as a material for a steel pipe for use in, for example, pipelines, oil country tubular goods, and civil engineering and construction, in particular, for a steel pipe of grade X80 specified in the API Standards by using conventional hot rolling equipment, which has a marked effect on the industry.
  • Description of Embodiments
  • The present invention will be specifically described hereafter.
  • First, the reasons for the limitations on the chemical composition of the hot-rolled steel sheet according to the present invention will be described. Hereinafter, % used below when describing a chemical composition always refers to mass%, unless otherwise noted.
  • C: 0.030% or more and 0.120% or less
  • C is a chemical element which is important for achieving the strength (tensile strength and yield strength) of a hot-rolled steel sheet by forming carbides with Nb, V, and Ti and which is indispensable for forming second phases (retained austenite and martensite) important for controlling the yield ratio of a hot-rolled steel sheet to be low. In order to achieve a desired strength and low yield ratio in the case of the hot-rolled steel sheet according to the present invention, it is necessary that the C content be 0.030% or more. On the other hand, in the case where the C content is more than 0.120%, there is a decrease in the toughness of the hot-rolled steel sheet due to an excessive increase in the amount of carbides. Also, in the case where the C content is more than 0.120%, since a carbon equivalent is high, there is a decrease in the toughness of a welded part when such a hot-rolled steel sheet is subjected to pipe making and welding. Therefore, the C content is set to be 0.030% or more and 0.120% or less, or preferably 0.040% or more and 0.090% or less.
  • Si: 0.05% or more and 0.50% or less
  • In the case where there is an increase in the Si content, Mn-Si-based non-metal inclusions are formed, which results in a decrease in the toughness of a welded part when such a hot-rolled steel sheet is subjected to pipe making and welding. Therefore, the upper limit of the Si content is set to be 0.50%. On the other hand, the lower limit of the Si content is set to be 0.05% in order to achieve the strength of grade X80 through solid solution strengthening. Here, it is preferable that the Si content be 0.10% or more and 0.35% or less.
  • Mn: 1.00% or more and 2.20% or less
  • Mn is a chemical element which is necessary for achieving the strength and the toughness of a hot-rolled steel sheet by inhibiting the formation of polygonal ferrite. Also, Mn is a chemical element which is necessary for achieving the low-yield-ratio property of a hot-rolled steel sheet by promoting the formation of second phases and by stably forming retained austenite and martensite. In order to realize such effects, it is necessary that the Mn content be 1.00% or more. On the other hand, in the case where the Mn content is more than 2.20%, there is a tendency for a variation in the mechanical properties of a hot-rolled steel sheet to occur due to center segregation and there is a decrease in toughness. Also, in the case where the Mn content is more than 2.20%, there may be a negative effect such as a decrease in elongation capability due to an increase in the strength of a hot-rolled steel sheet, and there may be a decrease in the toughness of a welded part due to an increase in carbon equivalent. Therefore, the Mn content is set to be 1.00% or more and 2.20% or less, or preferably 1.40% or more and 2.00% or less.
  • P: 0.025% or less, S: 0.0050% or less, and N: 0.0060% or less
  • Since P, which is present in steel as an impurity, is a chemical element which tends to be segregated, P causes a decrease in the toughness of a hot-rolled steel sheet. Therefore, the upper limit of the P content is set to be 0.025%, or preferably 0.018%.
  • Since S and N, like P, decrease the toughness of a hot-rolled steel sheet, the upper limit of the S content is set to be 0.0050%, and the upper limit of the N content is set to be 0.0060%. It is preferable that the S content be 0.0030% or less and that the N content be 0.0040% or less.
  • Here, the lower limits of the contents of P, S, and N are all decided in consideration of the practical limit of the control capability of a steel making process, it is preferable that the lower limits of each of the P content and the N content be 0.0010% and that the lower limit of the S content be 0.0001%.
  • Al: 0.005% or more and 0.100% or less
  • Al is effective as a deoxidizing agent for steel, and the Al content is set to be 0.005% or more with which the effect of deoxidizing is realized. However, in the case where the Al content is excessively large, alumina-based inclusions are formed, which results in defects occurring in a welded part when a hot-rolled steel sheet is subjected to welding. Therefore, the Al content is set to be 0.005% or more and 0.100% or less, or preferably 0.010% or more and 0.050% or less.
  • Nb: 0.020% or more and 0.100% or less
  • Nb is effective for decreasing a grain diameter and is a precipitation strengthening chemical element, and it is necessary that the Nb content be 0.020% or more in order to achieve a steel pipe strength of grade X80. On the other hand, in the case where the Nb content is excessively large, there is a decrease in toughness due to excessive precipitation in the coiling temperature range described below (400°C or higher and 650°C or lower) when a hot-rolled steel sheet is manufactured, and there is a decrease in weldability. Therefore, the Nb content is set to be 0.020% or more and 0.100% or less, or preferably 0.030% or more and 0.080% or less.
  • Mo: 0.05% or more and 0.50% or less
  • Mo is a chemical element which is effective for increasing the strength of a hot-rolled steel sheet by inhibiting austenite in a steel sheet from transforming into polygonal ferrite or pearlite in a cooling process following a hot rolling process when a hot-rolled steel sheet is manufactured. In addition, Mo is a chemical element which is necessary to achieve a satisfactory low-yield-ratio property of a hot-rolled steel sheet by promoting the formation of second phases (retained austenite and martensite). In order to realize such effects, the Mo content is set to be 0.05% or more. However, since Mo has a strong hardenability, in the case where the Mo content is more than 0.50%, there is a decrease in the toughness of a hot-rolled steel sheet due to the formation of excessive amounts of retained austenite and martensite, which are second phases. Therefore, the Mo content is set to be 0.05% or more and 0.50% or less, or preferably 0.10% or more and 0.35% or less.
  • Ti: 0.001% or more and 0.100% or less
  • Ti is a chemical element which is effective for decreasing a grain diameter and a precipitation strengthening chemical element, and it is necessary that the Ti content be 0.001% or more in order to realize such effects. On the other hand, in the case where the Ti content is excessively large, there is a decrease in the weldability of a hot-rolled steel sheet. Therefore, the Ti content is set to be 0.001% or more and 0.100% or less, or preferably 0.010% or more and 0.040% or less.
  • Cr: 0.05% or more and 0.50% or less
  • Cr is a chemical element which is effective for delaying pearlite transformation in a cooling process following a hot rolling process when a hot-rolled steel sheet is manufactured and which is effective for decreasing the amount of intergranular cementite. In addition, Cr is a chemical element which is necessary to achieve the low-yield-ratio property of a hot-rolled steel sheet by promoting the formation of retained austenite and martensite, which are second phases. In order to realize such effects, the Cr content is set to be 0.05% or more. On the other hand, in the case where the Cr content is more than 0.50%, there is a decrease in the toughness of a hot-rolled steel sheet due to the formation of excessive amounts of retained austenite and martensite, which are second phases. In addition, in the case where the Cr content is excessively large, there is a decrease in the toughness of a welded part due to the formation of a hardened structure in a welded part when a hot-rolled steel sheet is subjected to pipe making and welding. Therefore, the Cr content is set to be 0.05% or more and 0.50% or less, or preferably 0.10% or more and 0.35% or less.
  • Ca: 0.0005% or more and 0.0050% or less
  • Ca is effective for increasing the toughness of a hot-rolled steel sheet by inhibiting the formation of MnS as a result of fixing S. In order to realize such an effect, the Ca content is set to be 0.0005% or more. On the other hand, since there is a decrease in the toughness of a hot-rolled steel sheet due to the formation of Ca-based oxides in the case where the Ca content is excessively large, the Ca content is set to be 0.0050% or less. It is preferable that the Ca content be 0.0010% or more and 0.0030% or less.
  • Although the chemical composition described above is the basic chemical composition of a hot-rolled steel sheet according to the present invention, one, two, or more selected from among V: 0.001% or more and 0.100% or less, Cu: 0.001% or more and 0.50% or less, Ni: 0.001% or more and 1.00% or less, and B: 0.0040% or less may be added in addition to the basic chemical composition described above.
  • V: 0.001% or more and 0.100% or less
  • V is a precipitation strengthening chemical element, and it is preferable that the V content be 0.001% or more in order to realize such an effect. On the other hand, in the case where the V content is excessively large, since an excessive amount of precipitates is formed in the coiling temperature range (400°C or higher and 650°C or lower) described below when a hot-rolled steel sheet is manufactured, there may be a decrease in toughness and elongation property, and there may be a decrease in weldability. Therefore, it is preferable that the V content be 0.001% or more and 0.100% or less, or more preferably 0.020% or more and 0.080% or less.
  • Cu: 0.001% or more and 0.50% or less
  • Cu is a chemical element which is effective for inhibiting austenite in a steel sheet from transforming into polygonal ferrite or pearlite in a cooling process following a hot rolling process when a hot-rolled steel sheet is manufactured and which is effective for increasing the strength of a hot-rolled steel sheet. In order to realize such effects, it is preferable that the Cu content be 0.001% or more. However, in the case where the Cu content is more than 0.50%, there may be a decrease in the hot workability of steel. Therefore, it is preferable that the Cu content be 0.001% or more and 0.50% or less, or more preferably 0.10% or more and 0.40% or less.
  • Ni: 0.001% or more and 1.00% or less
  • Ni is a chemical element which is effective for inhibiting austenite in a steel sheet from transforming into polygonal ferrite or pearlite in a cooling process following a hot rolling process when a hot-rolled steel sheet is manufactured and which is effective for increasing the strength of a hot-rolled steel sheet. In order to realize such effects, it is preferable that the Ni content be 0.001% or more. However, in the case where the Ni content is more than 1.00%, there may be a decrease in the hot workability of steel. Therefore, it is preferable that the Ni content be 0.001% or more and 1.00% or less, or more preferably 0.10% or more and 0.50% or less.
  • B: 0.0040% or less
  • B is effective for preventing the formation of polygonal ferrite by inhibiting ferrite transformation at a high temperature in a cooling process following finish rolling when a hot-rolled steel sheet is manufactured. In order to realize such an effect, it is preferable that the B content be 0.0001% or more. On the other hand, in the case where the B content is excessively large, a hardened structure may be formed in a welded part when a hot-rolled steel sheet is subjected to welding. Therefore, it is preferable that the B content be 0.0040% or less, or more preferably 0.0002% or more and 0.0010% or less.
  • Here, in the case of the hot-rolled steel sheet according to the present invention, constituent chemical elements other than those described above are Fe and inevitable impurities. Examples of the inevitable impurities include Co, W, Pb, and Sn, and it is preferable that the content of each of these chemical elements be 0.02% or less.
  • Hereafter, the reasons for the limitations on the microstructure of the hot-rolled steel sheet according to the present invention will be described.
  • The hot-rolled steel sheet according to the present invention has a microstructure including bainitic ferrite as a main phase and martensite and retained austenite as second phases, in which the volume fraction of the main phase is 90% or more, in which the average grain diameter of the main phase is 10 µm or less, in which the volume fraction of the martensite is 0.5% or more and 9.5% or less, and in which the volume fraction of the retained austenite is 0.5% or more and 9.5% or less. Here, in the present invention, bainitic ferrite is a microstructure including a substructure having a high dislocation density in which cementite is not precipitated in grains. In contrast, bainite is different from bainitic ferrite in that bainite includes a lath structure having a high dislocation density in which cementite is precipitated in grains. In addition, polygonal ferrite is different from bainitic ferrite in that polygonal ferrite has a very low dislocation density.
  • Volume fraction of bainitic ferrite: 90% or more Average grain diameter of bainitic ferrite: 10 µm or less
  • In the present invention, by controlling the main phase of a hot-rolled steel sheet to be a fine bainitic ferrite excellent in terms of strength-toughness balance, the hot-rolled steel sheet is provided with a desired strength and low-temperature toughness. By controlling the volume fraction of bainitic ferrite, which is a main phase, to be 90% or more, and by controlling the average grain diameter of the bainitic ferrite to be 10 µm or less, it is possible to achieve satisfactory strength and low-temperature toughness of a hot-rolled steel sheet through the effect of a decrease in grain diameter. On the other hand, in the case where the volume fraction of bainitic ferrite is less than 90%, since there is an increase in the number of crack propagation paths due to an increase in the volume fraction of second phases, there is a decrease in the low-temperature toughness of a hot-rolled steel sheet. In addition, in the case where the average grain diameter of bainitic ferrite is more than 10 µm, there is a decrease in toughness due to an increase in fracture facet size.
  • Here, in order to achieve satisfactory strength and low-temperature toughness of a hot-rolled steel sheet, it is preferable that the volume fraction of bainitic ferrite be 91% or more, and it is preferable that the average grain diameter of bainitic ferrite be 3.0 µm or less. In particular, in the present invention, since martensite and retained austenite, which decrease toughness, are included, it is preferable that the average grain diameter of bainitic ferrite be 3.0 µm or less in the case where the total volume fraction of martensite and retained austenite is 4.0% or more. However, since there is a significant decrease in the volume fraction of second phases (retained austenite and martensite), which are important for decreasing the yield ratio of a hot-rolled steel sheet, in the case where the volume fraction of bainitic ferrite is excessively large, it is preferable that the volume fraction of bainitic ferrite be 95% or less. In addition, although it is preferable that the grain diameter of bainitic ferrite be as small as possible, the lower limit of the average grain diameter thereof is substantially about 1 µm.
  • Volume fraction of retained austenite: 0.5% or more and 9.5% or less
  • Since retained austenite undergoes strain-induced transformation due to forming strain, for example, when pipe making is performed, in sequence starting from a portion having a lower C concentration, there is an increase in work hardenability in a wide forming-strain range (for example, a forming-strain range of 1% to about 10%) corresponding to strain applied in a pipe making process. Therefore, since it is possible to increase tensile strength compared with yield strength, it is possible to achieve a low yield ratio. As a result, for example, even in the case of an electric resistance welded steel pipe where forming strain due to pipe making varies in the circumferential direction of the pipe, it is possible to stably achieve a low-yield-ratio property independently of location in the circumferential direction. In order to realize such an effect, it is necessary that the volume fraction of retained austenite be 0.5% or more, or preferably 2.0% or more. On the other hand, in the case where the volume fraction of retained austenite is more than 9.5%, since retained austenite functions as a crack propagation path, there is a decrease in the low-temperature toughness of a hot-rolled steel sheet. Therefore, it is necessary that the volume fraction of retained austenite be 9.5% or less. Here, it is preferable that the volume fraction of retained austenite be 5% or less in order to achieve further increased low-temperature toughness.
  • Volume fraction of martensite: 0.5% or more and 9.5% or less
  • Martensite increases the Bauschinger effect by facilitating the formation of movable dislocations during processing into bainitic ferrite. In order to realize such an effect, it is necessary that the volume fraction of martensite be 0.5% or more, or preferably 2.5% or more. On the other hand, in the case where the volume fraction of martensite is more than 9.5%, since martensite functions as a crack propagation path, there is a decrease in the low-temperature toughness of a hot-rolled steel sheet. Therefore, it is necessary that the volume fraction of martensite be 9.5% or less. Here, it is preferable that the volume fraction of martensite be 5% or less in order to achieve further increased low-temperature toughness.
  • Here, the microstructure of the hot-rolled steel sheet according to the present invention may include pearlite and cementite in addition to bainitic ferrite, retained austenite, and martensite described above. It is preferable that the volume fraction of the microstructures other than bainitic ferrite, retained austenite, and martensite, that is, pearlite and cementite be limited to 2% or less in total. In addition, it is preferable that the thickness of the hot-rolled steel sheet according to the present invention to be used as a material mainly for a linepipe be 15 mm or more and 30 mm or less.
  • Hereafter, the method for manufacturing the hot-rolled steel sheet according to the present invention will be described.
  • It is possible to manufacture the hot-rolled steel sheet according to the present invention by cooling a slab (cast piece) having the chemical composition described above which has been obtained by using a continuous casting method to a specified temperature or less, by then heating the cooled slab, by then performing rough rolling and finish rolling on the heated slab, by then performing accelerated cooling on the rolled steel sheet under specified conditions, and by then coiling the cooled steel sheet at a specified temperature in order to obtain a coil having a specified weight and width.
  • Cooling temperature of a continuously cast slab: 600°C or lower
  • A continuously cast slab which has not undergone ferrite transformation has an austenite structure and has a very large grain diameter because it has been exposed to a high temperature for a long time. Therefore, such a large austenite grain diameter is decreased through ferrite transformation. Therefore, the continuously cast slab is cooled to a temperature of 600°C or lower, or preferably 500°C or lower, at which ferrite transformation is almost completed. Here, subsequently, the continuously cast slab is heated so as to undergo reverse transformation into austenite, which results in a further decrease in grain diameter.
  • Heating temperature of a continuously cast slab: 1050°C or higher and 1300°C or lower
  • In the case where a slab heating temperature (reheating temperature of a continuously cast slab) is lower than 1050°C, since Nb, V, and Ti, which are precipitation strengthening chemical elements, do not sufficiently form a solid solution, it is not possible to achieve steel pipe strength of grade X80. On the other hand, in the case where the heating temperature is higher than 1300°C, since there is an increase in austenite grain diameter, and since, as a result, there is an increase in bainitic ferrite grain diameter, there is a decrease in the low-temperature toughness of a hot-rolled steel sheet, and there is a decrease in the toughness and elongation property of a hot-rolled steel sheet because an excessive amount of Nb is precipitated in cooling and coiling processes following a finish rolling process. Therefore, the reheating temperature of a continuously cast slab is set to be 1050°C or higher and 1300°C or lower, or preferably 1150°C or higher and 1230°C or lower.
  • The heated slab (continuously cast piece) is subjected to rough rolling and finish rolling so as to have an arbitrary thickness, and there is no particular limitation on what condition is used for rough rolling in the present invention.
  • Rolling reduction in the non-recrystallization temperature range when finish rolling is performed: 20% or more and 85% or less
  • By performing finish rolling in the non-recrystallization temperature range (about 930°C or lower in the steel chemical composition of the present invention), since strain is accumulated due to the delay of the recrystallization of austenite, there is a decrease in ferrite (bainitic ferrite) grain diameter when γ/α transformation occurs, which results in an increase in the strength and toughness of a hot-rolled steel sheet. Here, in the case where the rolling reduction in the non-recrystallization temperature range when finish rolling is performed is less than 20%, such an effect is not sufficiently realized. On the other hand, in the case where the rolling reduction described above is more than 85%, there is a problem in rolling due to an increase in resistance to deformation. Therefore, in the present invention, the rolling reduction described above is set to be 20% or more and 85% or less, or preferably 35% or more and 75% or less.
  • Finishing delivery temperature: equal to or higher than (Ar3 - 50°C) and equal to or lower than (Ar3 + 100°C)
  • In order to finish rolling with a uniform grain diameter and microstructure being obtained, it is necessary that the finishing delivery temperature be equal to or higher than (Ar3 - 50°C). In the case where the finishing delivery temperature is lower than (Ar3 - 50°C), since ferrite transformation occurs inside a hot-rolled steel sheet during a finish rolling process, polygonal ferrite is partially formed. Polygonal ferrite has a larger grain diameter than that of bainitic ferrite which is formed during a subsequent cooling process or after the cooling has been performed, which results in the formation of a mixed grain structure having a variation in grain diameter. Therefore, it is not possible to achieve desired properties of a hot rolled steel sheet. On the other hand, the finishing delivery temperature is higher than (Ar3 + 100°C), since there is an increase in bainitic ferrite grain diameter, there is a decrease in the toughness of a hot-rolled steel sheet. In particular, in the present invention, since martensite and retained austenite, which have a negative effect on toughness, are included in addition to bainitic ferrite, it is necessary to decrease a bainitic ferrite grain diameter in order to achieve satisfactory toughness. Therefore, the finishing delivery temperature is set to be equal to or higher than (Ar3 - 50°C) and equal to or lower than (Ar3 + 100°C), or preferably equal to or higher than (Ar3 - 20°C) and equal to or lower than (Ar3 + 50°C).
  • Here, the "finishing delivery temperature" refers to the surface temperature of a steel sheet determined at the exit of a finish rolling mill.
  • After finish rolling has been performed, accelerated cooling is performed under the following conditions. It is preferable that accelerated cooling be started within 7 seconds, or more preferably within 3 seconds, after finish rolling has been performed. In the case where the time until accelerated cooling is started after finish rolling has been performed is more than 7 seconds, there may be an increase in grain diameter, or ferrite transformation may start so that polygonal ferrite is formed.
  • Average cooling rate at the central position in the thickness direction of the steel sheet in a temperature range from the cooling start temperature to 650°C: 10°C/s or more and 100°C/s or less
  • In order to achieve satisfactory low-temperature toughness of a hot-rolled steel sheet by controlling the volume fraction of bainitic ferrite to be 90% or more as a result of inhibiting pearlite transformation and the formation of polygonal ferrite, it is necessary that an average cooling rate at the central position in the thickness direction of the steel sheet in a temperature range from the cooling start temperature to 650°C be 10°C/s or more. However, in the case where the cooling rate at the central position in the thickness direction of the steel sheet in the temperature range described above is excessively high, since there is an increase in the surface hardness of the steel sheet, the steel sheet is unsuitable for a steel sheet for a linepipe. Therefore, it is necessary that the upper limit of the average cooling rate described above be 100°C/s. It is preferable that the average cooling rate be 25°C/s or more and 50°C/s or less.
  • Cooling stop temperature at the central position in the thickness direction of the steel sheet: 420°C or higher and 650°C or lower
  • In order to disperse retained austenite and martensite in a microstructure as second phases, it is necessary to retain untransformed austenite by leaving the transformation of austenite in a steel sheet (austenite-to-bainitic ferrite transformation) unfinished in the cooling process. Therefore, in the range of the chemical composition according to the present invention, it is necessary that the temperature at which accelerated cooling is stopped be 420°C or higher in terms of the temperature at the central position in the thickness direction of the steel sheet. On the other hand, in the case where the temperature at which accelerated cooling is stopped is higher than 650°C, since polygonal ferrite and pearlite having a large grain diameter are formed, it is not possible to achieve a desired microstructure of a hot-rolled steel sheet. Therefore, it is necessary that the cooling stop temperature of accelerated cooling be 420°C or higher and 650°C or lower, or preferably 500°C or higher and 590°C or lower, in terms of the temperature at the central position in the thickness direction of the steel sheet.
  • Coiling temperature: 400°C or higher and 650°C or lower
  • In the present invention, austenite and martensite, which are second phases, are formed in an air cooling process following a coiling process. Therefore, it is necessary that C be diffused from bainitic ferrite, which is formed through transformation in the accelerated cooling process or after cooling has been stopped, to untransformed austenite. In the case where C is diffused from bainitic ferrite to untransformed austenite, since C is concentrated in the untransformed austenite, the untransformed austenite is inhibited from transforming into bainite, which results in martensite or retained austenite (untransformed austenite cooled to room temperature with the microstructure being unchanged) being obtained from the untransformed austenite. Whether martensite or retained austenite is obtained depends on the degree of the C concentration, and retained austenite is obtained in a portion in which there is an increase in C concentration so that the Ms point (temperature at which martensite transformation starts) is lower than room temperature.
  • In order to form a microstructure including a desired volume fractions of retained austenite and martensite by diffusing a sufficient amount of C in an air cooling process following a coiling process, it is necessary that the coiling temperature be 400°C or higher. On the other hand, in the case where the coiling temperature is higher than 650°C, since polygonal ferrite and pearlite having a large grain diameter are formed, it is not possible to achieve a desired microstructure of a hot-rolled steel sheet. Therefore, it is necessary that the coiling temperature be 400°C or higher and 650°C or lower, or preferably 480°C or higher and 580°C or lower. Here, the "coiling temperature" described above refers to the temperature at the central position in the thickness direction of the steel sheet in any case.
  • Coil weight after coiling has been performed: 20 tons or more Coil width after coiling has been performed: 1000 mm or more
  • In the present invention, it is necessary to disperse both retained austenite and martensite as second phase structures in a hot-rolled steel sheet by transforming a part of austenite retained in the untransformed state into martensite in an air cooling process following a coiling process. Here, in order to disperse a desired volume fraction of retained austenite and martensite as second phases, a cooling rate after coiling has been performed is very important.
  • In order to form a microstructure including a desired volume fraction of retained austenite and martensite, it is preferable to promote the diffusion of C from bainitic ferrite to untransformed austenite by decreasing a cooling rate as much as possible after coiling has been performed. However, in the case where the cooling rate is controlled by performing, for example, furnace cooling, it is necessary to newly install, for example, a cooling furnace to the rolling equipment, there is a disadvantage from the viewpoint of equipment costs. Therefore, in the present invention, by specifying coil weight and coil width after coiling has been performed, an air cooling rate is decreased after coiling has been performed.
  • In order to sufficiently decrease an air cooling rate after coiling has been performed by decreasing the ratio of (surface area)/(volume) of a coil, it is necessary that the coil weight be 20 tons or more and the coil width be 1000 mm or more. In the case where the coil weight after coiling has been performed is less than 20 tons or the coil width after coiling has been performed is less than 1000 mm, since the amount of C concentrated is not sufficient for austenite retained in the untransformed state to be stable due to excessive large air cooling rate after coiling has been performed, only martensite is preferentially formed as a second phase. As a result, since there is an insufficient amount of retained austenite in a hot-rolled steel sheet, it is not possible to achieve stable low-yield-ratio property in a wide forming-strain range. In order to achieve the amount of retained austenite according to the present invention, it is preferable that the air cooling rate after coiling has been performed be 70°C/s or less, or more preferably 50°C/s or less. Here, the "air cooling rate after coiling has been performed" refers to an average cooling rate in a temperature range of 400°C to 390°C in terms of the temperature of a steel sheet. The temperature of a coil is determined at the central position in the width direction of the peripheral surface of the coil after coiling has been performed. The temperature of a coil is determined by using a thermocouple that is attached to a proper portion of the steel sheet where the steel sheet is coiled tightly such that no air gap is formed therein, the portion being positioned at the center in the width direction of the peripheral surface of the steel sheet. In addition, the reason for defining an air cooling rate after coiling has been performed as an average cooling rate in a temperature range of 400°C to 390°C is because C is most likely to be concentrated in austenite retained in the untransformed state in a temperature range around 400°C.
  • For the reasons described above, the coil weight after coiling has been performed is set to be 20 tons or more and the coil width after coiling has been performed is set to be 1000 mm or more. In addition, it is preferable that the coil weight after coiling has been performed be 25 tons or more and the coil width after coiling has been performed be 1400 mm or more. Although there is no particular limitation on the upper limits of the coil weight and the coil width after coiling has been performed, considering the operation records of the rolling equipment, the substantial upper limits of the coil weight and coil width are respectively about 40 tons and about 2500 mm.
  • EXAMPLES
  • By casting slabs (continuously cast piece having a thickness of 215 mm) having the chemical compositions given in Table 1, by cooling the cast slabs to a temperature of about 400°C or lower, by further performing hot rolling under the hot rolling conditions given in Table 2, by cooling the hot-rolled steel sheet under the cooling conditions given in Table 2 following the hot rolling, and by coiling the cooled steel sheet into coils having the specified sizes at a coiling temperatures given in Table 2, hot-rolled steel sheets (steel strips) having the thicknesses given in Table 2 were obtained. Here, the cooling described above (accelerated cooling) was started within 3 seconds after finish rolling had been performed. In addition, the Ar3 points given in Table 2 were determined from thermal expansion curves obtained by taking samples for thermal expansion determination from the obtained slabs, by transforming them into austenite at a temperature of 950°C, and by then cooling the samples at a cooling rate of 5°C/min.
  • By forming the obtained hot-rolled steel sheets (steel strips) by performing cage-roll forming, by performing electric resistance welding, by grinding the inner beads, by then performing a heat treatment only on the welded parts by using a post-annealing device, and by performing sizing, electric resistance welded steel pipes having an outer diameter of 16 inches were obtained.
  • Here, in the examples of the present invention, although a manufacturing method in which an electric resistance welded steel pipe is manufactured from a hot-rolled steel sheet was used, it is possible to use the hot-rolled steel sheet according to the present invention not only for an electric resistance welded steel pipe but also for various kinds of steel pipes such as a spiral steel pipe.
  • By taking test pieces from the obtained hot-rolled steel sheets and the electric resistance welded steel pipes, microstructure observation, a tensile test, and a Charpy impact test were performed. The methods for microstructure observation and the various tests were as follows.
  • (1) Microstructure observation
  • By observing the microstructures in the three or more fields of view each at the central position in the thickness direction of the obtained hot-rolled steel sheet, at a position of 1/4 of the thickness, at a position of 3/4 of the thickness, and at a position located at 1 mm from the surface of the steel sheet by using a scanning electron microscope (at a magnification of 2000 times) in order to obtain the photographs of the observed images, the volume fractions of bainitic ferrite, retained austenite, martensite, and pearlite were determined. Here, from the results of the microstructure observation of the obtained hot-rolled steel sheets, no microstructure other than bainitic ferrite, retained austenite, martensite, and pearlite was observed in the matrix in the case of the hot-rolled steel sheet of the examples of the present invention.
  • By performing image analysis on the photographs obtained as described above in order to separate bainitic ferrite from the microstructures other than bainitic ferrite, by determining the area ratio of bainitic ferrite in each field of view, the volume fraction of bainitic ferrite was defined as the average value of the area ratios determined at all of the positions in the thickness direction described above. In addition, by determining the area ratio of pearlite in each field of view by using the same method, the volume fraction of pearlite was defined as the average value of the area ratios determined at all of the positions in the thickness direction described above. Moreover, by using the same method, the volume fraction of polygonal ferrite was determined. The average grain diameter of bainitic ferrite was defined as the circle-equivalent diameter obtained by performing image analysis on the microstructures which were recognized as bainitic ferrite.
  • There is no distinct contrast between retained austenite and martensite under a scanning electron microscope. Therefore, first, by determining the total area ratio of retained austenite and martensite in each field of view by using the same method described above, the total volume fraction of retained austenite and martensite was defined as the average value of the area ratios determined at all of the positions in the thickness direction described above. Subsequently, by determining the volume fraction of retained austenite by using an X-ray diffraction method, the volume fraction of martensite was defined as the result of subtracting the volume fraction of retained austenite from the total volume fraction described above.
  • Here, the volume fraction of retained austenite was determined by using the X-ray diffraction method described below.
  • By taking an X-ray diffraction test piece in a direction parallel to the surface of the steel sheet, by performing grinding and chemical polishing on the test piece, a surface at a position of 1/4 of the thickness of the steel sheet was exposed as the surface of the polished test piece. Subsequently, by determining the diffraction intensities of the (200) plane and (211) plane of α and the (200) plane, (220) plane, and (311) plane of γ by the X-ray diffraction analysis for the test pieces, the volume fraction of γ was calculated.
  • (2) Tensile test
  • By taking a full-thickness flat tensile test piece (having a thickness equal to the full-thickness of the steel sheet, a length of the parallel portion of 60 mm, a gauge length of 50 mm, and a gauge width of 38 mm) from the central position in the width direction of the obtained hot-rolled steel sheet so that the longitudinal direction of the test piece was a direction (C-direction) at a right angle to the rolling direction, and by performing a tensile test at room temperature in accordance with the prescription in ASTM E8M-04 in order to determine tensile strength TS and yield strength YS, a yield ratio YR (= YS/TS) was derived. In addition, after having flattening the obtained electric resistance welded steel pipe, tensile test pieces having the same shape as described above were taken from the position located at 90 degrees and the position located at 180 degrees in the circumferential direction from the welded part which was assumed to be located at 0 degrees so that the longitudinal direction of the test pieces was the circumferential direction of the steel pipe. Subsequently, by deriving yield ratios by performing a tensile test under the same conditions described above, the difference in yield ratio ΔYR between the position located at 90 degrees and the position located at 180 degrees which were different in forming strain from each other. A case where the tensile strength TS, yield strength YS, and yield ratio YR of a hot-rolled steel sheet were respectively 650 MPa or more, 555 MPa or more, and 90% or less and where the difference ΔYR in yield ratio between the position at 90 degrees and the position at 180 degrees of an electric resistance welded steel pipe was less than 10% was judged as the case of "tensile properties excellent in terms of strength, stability of properties after processing has been performed, and low-yield-ratio property".
  • (3) Charpy impact test
  • By taking a V-notch test piece (having a length of 55 mm, a height of 10 mm, and a width of 10 mm) from the central position in the thickness direction of the obtained hot-rolled steel sheet so that the longitudinal direction of the test piece was a direction (C-direction) at a right angle to the rolling direction, and by performing a Charpy impact test in accordance with the prescription in JIS Z 2242, a ductile-brittle transition temperature (°C) was determined. Here, three test pieces were taken from each of the hot-rolled steel sheets, and the ductile-brittle transition temperature (vTrs) of each of the hot-rolled steel sheet was defined as the arithmetic average value of the obtained ductile-brittle transition temperatures of the three test pieces. A case where vTrs was -80°C or lower was judged as the case of "good toughness". [Table 1]
    Steel No. Chemical Composition (mass %) Note
    C Si Mn P S Al N Nb Mo Ti Cr Ca Other
    1 0.066 0.22 1.74 0.016 0.0022 0.030 0.0026 0.055 0.25 0.014 0.14 0.0020 - Example Steel
    2 0.080 0.25 1.89 0.011 0.0025 0.031 0.0030 0.079 0.29 0.019 0.29 0.0023 - Example Steel
    3 0.039 0.29 1.91 0.015 0.0022 0.031 0.0022 0.042 0.13 0.035 0.09 0.0024 - Example Steel
    4 0.034 0.19 1.55 0.016 0.0025 0.026 0.0034 0.031 0.31 0.022 0.11 0.0018 V:0.061 Example Steel
    5 0.051 0.23 2.05 0.012 0.0025 0.030 0.0020 0.055 0.09 0.013 0.26 0.0018 Cu:0.35, Ni:0.34 Example Steel
    6 0.069 0.24 1.99 0.017 0.0018 0.029 0.0025 0.049 0.17 0.011 0.17 0.0016 B:0.0009 Example Steel
    7 0.085 0.16 1.57 0.012 0.0022 0.033 0.0032 0.067 0.03 0.020 0.16 0.0015 B:0.0002 Comparative Steel
    8 0.051 0.30 1.62 0.020 0.0018 0.031 0.0031 0.039 0.11 0.029 0.03 0.0015 Cu:0.11, Ni:0.11 Comparative Steel
    9 0.035 0.22 1.46 0.018 0.0025 0.028 0.0022 0.052 0.55 0.019 0.10 0.0020 - Comparative Steel
    10 0.046 0.33 1.67 0.016 0.0018 0.027 0.0023 0.060 0.12 0.015 0.56 0.0024 - Comparative Steel
    [Table 2]
    Steel Sheet No. Steel No. Ar3 Point (°C) Slab Reheating Temperature (°C) Finish Rolling Condition Cooling Start Temperature *1 (°C) Average Cooling Rate*2 (°C/s) Cooling Stop Temperature*3 (°C) Coiling Temperature*4 (°C) Air cooling Rate after Coiling*5 (°C/s) Coil Size after Coiling Note
    Finishing Delivery Temperature (°C) Rolling Reduction in Non-recrystallization Range (%) Coil Weight (ton) Coil width (mm) Thickness (mm)
    1A 1 729 1200 761 60 770 36 539 525 48 29 2100 25 Example
    1B 729 1200 775 60 790 33 516 505 74 13 1350 16 Comparative Example
    2A 2 714 1210 759 60 770 27 502 490 66 28 2440 17 Example
    2B 714 1210 774 60 780 28 672 660 44 32 1900 29 Comparative Example
    3A 3 730 1200 716 60 730 26 510 500 50 32 1470 20 Example
    3B 730 1200 775 60 780 35 572 560 82 34 900 20 Comparative Example
    4A 4 754 1190 736 60 750 33 540 520 44 24 1610 23 Example
    5A 5 714 1220 763 60 780 29 586 570 50 31 1460 15 Example
    6A 6 711 1150 720 60 740 17 432 420 45 23 1870 19 Example
    7A 7 732 1230 752 60 760 16 538 520 46 31 1830 21 Comparative Example
    8A 8 745 1260 767 60 770 16 618 600 45 35 1540 21 Comparative Example
    9A 9 760 1200 800 60 810 39 581 570 61 33 2270 22 Comparative Example
    10A 10 744 1210 806 60 815 38 559 540 48 31 1810 22 Comparative Example
    *1) Cooling start temperature at the central position in the thickness direction
    *2) Average cooling rate from cooling stat temperature to 650°C at the central position in the thickness direction
    *3) Cooling stop temperature at the central position in the thickness direction
    *4) Coiling temperature at the central position in the thickness direction
    *5) Average cooling rate from 400°C to 390°C at the central position in the width direction of the peripheral surface of a coil
    [Table 3]
    Steel Sheet No. Steel No. Microstructure of Hot-rolled Steel Sheet Mechanical Property Note
    Bainitic Ferrite Retained Austenite Volume Fraction (%) Martensite Volume Fraction (%) Pearlite Volume Fraction (%) Polygonal Ferrite Volume Fraction (%) Hot-rolled Steel Sheet (Width Direction) Electric Resistance Welded Steel Pipe (Peripheral Direction of Steel Pipe)
    Average Grain Diameter (µm) Volume Fraction (%) Yield Strength YS (MPa) Tensile Strength TS (MPa) Yield Ratio YR (%) vTrs (°C) Yield Ratio (%) Difference in Yield Ratio ΔYR*8 (%)
    90-Degree YR90*6 180-Degree YR180*7
    1A 1 3.0 93.2 2.7 3.0 1.1 0.0 593 754 79 -120 81 83 2 Example
    1B 2.9 93.3 0.4 5.1 1.2 0.0 580 743 78 -120 81 93 12 Comparative Example
    2A 2 2.1 90.9 3.8 3.8 1.5 0.0 648 868 75 -120 76 82 6 Example
    2B 2.7 86.7 0.8 1.1 5.2 6.2 520 693 75 -75 74 85 11 Comparative Example
    3A 3 3.0 93.3 3.0 2.7 1.0 0.0 575 733 78 -130 82 89 7 Example
    3B 3.2 93.2 0.3 5.3 1.2 0.0 544 725 75 -130 79 93 14 Comparative Example
    4A 4 4.2 94.8 2.1 2.5 0.6 0.0 564 697 81 -130 80 87 7 Example
    5A 5 2.4 92.3 3.7 3.0 1.0 0.0 629 822 77 -120 81 87 6 Example
    6A 6 1.8 92.1 3.2 3.9 0.8 0.0 571 732 78 -130 80 83 3 Example
    7A 7 3.1 98.9 0.3 0.3 0.5 0.0 733 789 93 -115 83 94 11 Comparative Example
    8A 8 4.0 97.8 0.4 0.7 1.1 0.0 700 769 91 -120 84 95 11 Comparative Example
    9A 9 4.7 82.7 2.9 13.5 0.9 0.0 746 857 87 -55 81 85 4 Comparative Example
    10A 10 3.8 85.7 1.5 11.8 1.0 0.0 701 825 85 -50 85 91 6 Comparative Example
    *6) Yield Ratio YR90 (%) at the position located at 90 degrees in the circumferential direction from the welded part of the electric resistance welded steel pipe which is assumed to be located at 0 degrees
    *7) Yield Ratio YR180 (%) at the position located at 180 degrees in the circumferential direction from the welded part of the electric resistance welded steel pipe which is assumed to be located at 0 degrees
    *8) ΔYR (%) = |YR90 - YR180|
  • As Table 3 indicates, the hot-rolled steel sheets of the examples of the present invention were good in terms of all of tensile properties (yield strength, tensile strength, yield ratio, and the difference in yield ratio of an electric resistance welded steel pipe) and toughness (low-temperature toughness). In contrast, the hot-rolled steel sheets of the comparative examples were unsatisfactory in terms of one or both of tensile properties and toughness (low-temperature toughness).

Claims (3)

  1. A hot-rolled steel sheet having a chemical composition consisting of , by mass%,
    C: 0.030% or more and 0.120% or less, Si: 0.05% or more and 0.50% or less,
    Mn: 1.00% or more and 2.20% or less, P: 0.025% or less,
    S: 0.0050% or less, N: 0.0060% or less,
    Al: 0.005% or more and 0.100% or less, Nb: 0.020% or more and 0.100% or less,
    Mo: 0.05% or more and 0.50% or less, Ti: 0.001% or more and 0.100% or less,
    Cr: 0.05% or more and 0.50% or less, Ca: 0.0005% or more and 0.0050% or less,
    optionally one or more selected from among V: 0.001% or more and 0.100% or less, Cu: 0.001% or more and 0.50% or less, Ni: 0.001% or more and 1.00% or less, and B: 0.0040% or less, and the balance being Fe and inevitable impurities, and having a microstructure including, bainitic ferrite as a main phase and martensite and retained austenite as second phases,
    wherein the volume fraction of the main phase is 90% or more, the average grain diameter of the main phase is 10 µm or less, the volume fraction of the martensite is 0.5% or more and 9.5% or less, and the volume fraction of the retained austenite is 0.5% or more and 9.5% or less, wherein a yield ratio of 90% or less, a yield strength of 555 MPa or more, and a tensile strength of 650 MPa or more.
  2. The hot-rolled steel sheet according to Claim 1, the steel sheet having the chemical composition containing, by mass%, one or more selected from among V: 0.001% or more and 0.100% or less, Cu: 0.001% or more and 0.50% or less, Ni: 0.001% or more and 1.00% or less, and B: 0.0040% or less.
  3. A method for manufacturing a hot-rolled steel sheet according to claim 1 or 2, the method comprising: cooling a continuously cast slab having the chemical composition according to Claim 1 or 2 to a temperature of 600°C or lower; then heating the cooled slab in a temperature range of 1050°C or higher and 1300°C or lower; performing rough rolling; performing finish rolling following the rough rolling, wherein rolling reduction in a non-recrystallization temperature range is 20% or more and 85% or less, and wherein a finishing delivery temperature is equal to or higher than (Ar3 - 50°C) and equal to or lower than (Ar3 + 100°C) ; performing cooling following the finish rolling, wherein an average cooling rate at the central position in the thickness direction of the steel sheet is 10°C/s or more and 100°C/s or less in a temperature range from the cooling start temperature to 650°C, and wherein a cooling stop temperature is 420°C or higher and 650°C or lower; and performing coiling in a temperature range of 400°C or higher and 650°C or lower in order to obtain a coil having a weight of 20 tons or more and a width of 1000 mm or more.
EP14866276.0A 2013-11-28 2014-11-20 Hot-rolled steel sheet and method for manufacturing the same Active EP3040439B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2013245616A JP5783229B2 (en) 2013-11-28 2013-11-28 Hot-rolled steel sheet and manufacturing method thereof
PCT/JP2014/005836 WO2015079661A1 (en) 2013-11-28 2014-11-20 Hot-rolled steel sheet and method for manufacturing same

Publications (3)

Publication Number Publication Date
EP3040439A1 EP3040439A1 (en) 2016-07-06
EP3040439A4 EP3040439A4 (en) 2016-10-05
EP3040439B1 true EP3040439B1 (en) 2018-01-03

Family

ID=53198630

Family Applications (1)

Application Number Title Priority Date Filing Date
EP14866276.0A Active EP3040439B1 (en) 2013-11-28 2014-11-20 Hot-rolled steel sheet and method for manufacturing the same

Country Status (7)

Country Link
US (1) US10273554B2 (en)
EP (1) EP3040439B1 (en)
JP (1) JP5783229B2 (en)
KR (1) KR101802269B1 (en)
CN (1) CN105793458B (en)
TW (1) TWI558823B (en)
WO (1) WO2015079661A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111304516A (en) * 2020-03-05 2020-06-19 中天钢铁集团有限公司 Non-quenched and tempered steel for high-strength high-low-temperature impact toughness lifting hook and production process

Families Citing this family (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6070642B2 (en) * 2014-06-20 2017-02-01 Jfeスチール株式会社 Hot-rolled steel sheet having high strength and excellent low-temperature toughness and method for producing the same
CN104264054B (en) * 2014-09-19 2017-02-22 宝山钢铁股份有限公司 550MPa-level high-temperature resistant pipeline steel and preparation method thereof
JP6252692B2 (en) 2015-07-27 2017-12-27 Jfeスチール株式会社 High strength hot rolled steel sheet and method for producing the same
US11241726B2 (en) 2015-11-25 2022-02-08 Jfe Steel Corporation Hot-rolled steel sheet and method for manufacturing same
KR102348539B1 (en) * 2015-12-24 2022-01-07 주식회사 포스코 High strength steel having low yield ratio method for manufacturing the same
JP6519024B2 (en) * 2016-05-31 2019-05-29 Jfeスチール株式会社 Method of manufacturing low yield ratio high strength hot rolled steel sheet excellent in low temperature toughness
RU2699381C1 (en) 2016-06-22 2019-09-05 ДжФЕ СТИЛ КОРПОРЕЙШН Hot-rolled steel sheet for thick-walled high-strength main pipeline, welded steel pipes for thick-walled high-strength main pipeline and method of welded steel pipe manufacturing
CN106435369B (en) * 2016-11-29 2018-08-07 武汉钢铁有限公司 A kind of normalizing state of the excellent in low temperature toughness containing Cr is anti-corrosion wind-powered electricity generation steel and production method
JP6565890B2 (en) * 2016-12-20 2019-08-28 Jfeスチール株式会社 Low yield ratio and high strength hot rolled steel sheet with excellent low temperature toughness
JP6394841B1 (en) * 2017-02-17 2018-09-26 Jfeスチール株式会社 High strength hot rolled steel sheet and method for producing the same
KR101998952B1 (en) * 2017-07-06 2019-07-11 주식회사 포스코 Ultra high strength hot rolled steel sheet having low deviation of mechanical property and excellent surface quality, and method for manufacturing the same
JP6866933B2 (en) * 2017-11-24 2021-04-28 日本製鉄株式会社 Hot-rolled steel sheet and its manufacturing method
KR102020415B1 (en) * 2017-12-24 2019-09-10 주식회사 포스코 High strength steel sheet having excellent low yield ratio property, and manufacturing method for the same
JP6572963B2 (en) 2017-12-25 2019-09-11 Jfeスチール株式会社 Hot-rolled steel sheet and manufacturing method thereof
JP6635231B2 (en) * 2018-01-30 2020-01-22 Jfeスチール株式会社 Steel material for line pipe, method for manufacturing the same, and method for manufacturing line pipe
EP3733878B1 (en) * 2018-01-30 2021-10-13 JFE Steel Corporation Steel material for line pipes, production method for same, and production method for line pipe
CN110643894B (en) * 2018-06-27 2021-05-14 宝山钢铁股份有限公司 Ultra-high strength hot rolled steel sheet and steel strip having good fatigue and hole expansion properties, and method for manufacturing same
WO2020026594A1 (en) * 2018-07-31 2020-02-06 Jfeスチール株式会社 High-strength hot-rolled plated steel sheet
CN112585289B (en) * 2018-08-23 2022-04-29 杰富意钢铁株式会社 Hot-rolled steel sheet and method for producing same
JP6693606B1 (en) * 2018-08-23 2020-05-13 Jfeスチール株式会社 Square steel pipe, manufacturing method thereof, and building structure
KR102175575B1 (en) * 2018-11-26 2020-11-09 주식회사 포스코 Hot rolled steel sheet having excellent ductility and strength and method of manufacturing the same
EP3872205A4 (en) * 2019-02-19 2021-09-01 Nippon Steel Corporation Electric-resistance-welded steel pipe for line pipe
DE102019122515A1 (en) * 2019-08-21 2021-02-25 Ilsenburger Grobblech Gmbh Process for the production of high-strength sheets or strips from a low-alloy, high-strength bainitic steel and a steel strip or sheet steel from this
CN111155035A (en) * 2020-02-17 2020-05-15 本钢板材股份有限公司 Large-angle grain boundary extra-thick specification X80 pipeline steel and preparation method thereof
EP4139492A1 (en) * 2020-04-22 2023-03-01 ThyssenKrupp Steel Europe AG Hot-rolled flat steel product and method for the production thereof
CN114107794B (en) * 2020-08-31 2023-08-11 宝山钢铁股份有限公司 980 MPa-grade ultra-low carbon martensite and residual austenite ultra-high hole-enlarging steel and manufacturing method thereof
JP7081727B1 (en) * 2020-10-05 2022-06-07 Jfeスチール株式会社 Electric pipe and its manufacturing method
CN113549824A (en) * 2021-06-29 2021-10-26 武汉钢铁有限公司 Hot continuous rolling limit thickness specification high-strength pipeline steel plate coil and manufacturing method thereof
WO2023214472A1 (en) * 2022-05-06 2023-11-09 Jfeスチール株式会社 Hot-rolled steel sheet and method for manufacturing same, and electric resistance welded steel pipe and method for manufacturing same

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2510187B2 (en) 1987-03-17 1996-06-26 川崎製鉄株式会社 Method for producing hot-rolled steel sheet for low-yield ratio high-strength line pipe with excellent low temperature toughness
AU2783795A (en) * 1994-07-08 1996-02-09 Ipsco Inc. Twin-roll caster and rolling mill for use therewith
JP3589071B2 (en) 1998-03-24 2004-11-17 住友金属工業株式会社 Manufacturing method of ultra-thick section steel with excellent weldability, strength and toughness
CN100562601C (en) 2001-06-06 2009-11-25 新日本制铁株式会社 Have the high-strength hot-dip galvanized steel sheet of high binding force of cladding material behind fatigue resistance, erosion resistance, ductility and the severe deformation and the steel sheet and the manufacture method thereof of galvanizing layer DIFFUSION TREATMENT
JP5011773B2 (en) 2005-03-24 2012-08-29 Jfeスチール株式会社 Manufacturing method of low yield ratio ERW steel pipe with excellent low temperature toughness
JP2006299414A (en) * 2005-03-24 2006-11-02 Jfe Steel Kk Method for producing low yield-ratio electric-resistance welded steel tube excellent in low temperature toughness
JP5151008B2 (en) 2005-03-29 2013-02-27 Jfeスチール株式会社 Hot-rolled steel sheet for sour-resistant and high-strength ERW pipe with excellent HIC resistance and weld toughness and method for producing the same
JP4164537B2 (en) * 2006-12-11 2008-10-15 株式会社神戸製鋼所 High strength thin steel sheet
JP5499734B2 (en) * 2009-01-30 2014-05-21 Jfeスチール株式会社 Ultra-thick high-tensile hot-rolled steel sheet excellent in low-temperature toughness and method for producing the same
US8784577B2 (en) 2009-01-30 2014-07-22 Jfe Steel Corporation Thick high-tensile-strength hot-rolled steel sheet having excellent low-temperature toughness and manufacturing method thereof
JP5776398B2 (en) * 2011-02-24 2015-09-09 Jfeスチール株式会社 Low yield ratio high strength hot rolled steel sheet with excellent low temperature toughness and method for producing the same
JP5679114B2 (en) * 2011-02-24 2015-03-04 Jfeスチール株式会社 Low yield ratio high strength hot rolled steel sheet with excellent low temperature toughness and method for producing the same
JP5919920B2 (en) 2011-03-28 2016-05-18 Jfeスチール株式会社 Method and apparatus for producing Si-containing cold-rolled steel sheet
JP5776377B2 (en) 2011-06-30 2015-09-09 Jfeスチール株式会社 High-strength hot-rolled steel sheet for welded steel pipes for line pipes with excellent sour resistance and method for producing the same
JP5834717B2 (en) * 2011-09-29 2015-12-24 Jfeスチール株式会社 Hot-dip galvanized steel sheet having a high yield ratio and method for producing the same
JP5900303B2 (en) 2011-12-09 2016-04-06 Jfeスチール株式会社 High-strength steel sheet for sour-resistant pipes with excellent material uniformity in the steel sheet and its manufacturing method
JP2013155390A (en) * 2012-01-26 2013-08-15 Jfe Steel Corp High strength hot rolled steel sheet having excellent fatigue property and method for producing the same
JP2013204103A (en) * 2012-03-29 2013-10-07 Jfe Steel Corp High strength welded steel pipe for low temperature use having superior buckling resistance, and method for producing the same, and method for producing steel sheet for high strength welded steel pipe for low temperature use having superior buckling resistance

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
None *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111304516A (en) * 2020-03-05 2020-06-19 中天钢铁集团有限公司 Non-quenched and tempered steel for high-strength high-low-temperature impact toughness lifting hook and production process

Also Published As

Publication number Publication date
JP5783229B2 (en) 2015-09-24
TWI558823B (en) 2016-11-21
JP2015101781A (en) 2015-06-04
WO2015079661A1 (en) 2015-06-04
EP3040439A4 (en) 2016-10-05
CN105793458B (en) 2017-11-24
US10273554B2 (en) 2019-04-30
CN105793458A (en) 2016-07-20
TW201527848A (en) 2015-07-16
EP3040439A1 (en) 2016-07-06
US20160289788A1 (en) 2016-10-06
KR20160090363A (en) 2016-07-29
KR101802269B1 (en) 2017-11-28

Similar Documents

Publication Publication Date Title
EP3040439B1 (en) Hot-rolled steel sheet and method for manufacturing the same
EP3246427B1 (en) High strength electric resistance welded steel pipe and manufacturing method therefor
US10900104B2 (en) Hot rolled steel sheet and method for manufacturing the same
EP2735622B1 (en) Low-yield-ratio high-strength hot-rolled steel plate with excellent low-temperature toughness and process for producing same
EP2949772B1 (en) Hot-rolled steel sheet and method for manufacturing same
JP5776398B2 (en) Low yield ratio high strength hot rolled steel sheet with excellent low temperature toughness and method for producing the same
EP2392681B1 (en) Heavy gauge, high tensile strength, hot rolled steel sheet with excellent hic resistance and manufacturing method therefor
EP2505682B1 (en) Welded steel pipe for linepipe with superior compressive strength, and process for producing same
EP2871254B1 (en) Hot-rolled steel sheet and method for manufacturing same
JP6135577B2 (en) High strength hot rolled steel sheet and method for producing the same
EP2133441A1 (en) High-strength hot-rolled steel plate excellent in low-temperature toughness for spiral pipe and process for producing the same
EP2963138B1 (en) Production method for thick steel plate
EP3375900A1 (en) Electric resistance welded steel tube for line pipe
JP6519024B2 (en) Method of manufacturing low yield ratio high strength hot rolled steel sheet excellent in low temperature toughness
EP3276033B1 (en) High-strength steel, production method therefor, steel pipe, and production method for steel pipe
EP3276020A1 (en) High-strength steel, production method therefor, steel pipe, and production method therefor
CA3159223A1 (en) Electric resistance welded steel pipe, method for producing the same, line pipe, and building structure
EP3960891B1 (en) Electric resistance welded steel pipe for linepipe
JP2021172848A (en) Electroseamed steel pipe for linepipe, and hot-rolled steel sheet for linepipe
JP2021172849A (en) Electroseamed steel pipe for linepipe, and hot-rolled steel sheet for linepipe
Bagmet et al. Quality of thick steel sheet for spiral-seam electrowelded pipe of strength class K60 (X70)

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20160331

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

AX Request for extension of the european patent

Extension state: BA ME

REG Reference to a national code

Ref country code: DE

Ref legal event code: R079

Ref document number: 602014019568

Country of ref document: DE

Free format text: PREVIOUS MAIN CLASS: C22C0038000000

Ipc: C21D0008020000

A4 Supplementary search report drawn up and despatched

Effective date: 20160907

RIC1 Information provided on ipc code assigned before grant

Ipc: C22C 38/60 20060101ALI20160901BHEP

Ipc: C22C 38/46 20060101ALI20160901BHEP

Ipc: C22C 38/48 20060101ALI20160901BHEP

Ipc: C22C 38/04 20060101ALI20160901BHEP

Ipc: C21D 8/02 20060101AFI20160901BHEP

Ipc: C22C 38/44 20060101ALI20160901BHEP

Ipc: C21D 9/08 20060101ALI20160901BHEP

Ipc: C22C 38/22 20060101ALI20160901BHEP

Ipc: C22C 38/50 20060101ALI20160901BHEP

Ipc: C22C 38/38 20060101ALI20160901BHEP

Ipc: C22C 38/32 20060101ALI20160901BHEP

Ipc: C22C 38/58 20060101ALI20160901BHEP

Ipc: C22C 38/06 20060101ALI20160901BHEP

Ipc: C21D 9/46 20060101ALI20160901BHEP

Ipc: C22C 38/24 20060101ALI20160901BHEP

Ipc: C22C 38/54 20060101ALI20160901BHEP

Ipc: C22C 38/02 20060101ALI20160901BHEP

Ipc: C22C 38/26 20060101ALI20160901BHEP

DAX Request for extension of the european patent (deleted)
GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

INTG Intention to grant announced

Effective date: 20170901

RIN1 Information on inventor provided before grant (corrected)

Inventor name: SHIBATA, TOMOAKI

Inventor name: GOTO, SOTA

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

Ref country code: AT

Ref legal event code: REF

Ref document number: 960328

Country of ref document: AT

Kind code of ref document: T

Effective date: 20180115

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 602014019568

Country of ref document: DE

REG Reference to a national code

Ref country code: NL

Ref legal event code: MP

Effective date: 20180103

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG4D

REG Reference to a national code

Ref country code: AT

Ref legal event code: MK05

Ref document number: 960328

Country of ref document: AT

Kind code of ref document: T

Effective date: 20180103

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180103

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: HR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180103

Ref country code: LT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180103

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180103

Ref country code: NO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180403

Ref country code: ES

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180103

Ref country code: CY

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180103

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: AT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180103

Ref country code: PL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180103

Ref country code: RS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180103

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180404

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180103

Ref country code: LV

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180103

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180503

Ref country code: BG

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180403

REG Reference to a national code

Ref country code: DE

Ref legal event code: R097

Ref document number: 602014019568

Country of ref document: DE

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: AL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180103

Ref country code: IT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180103

Ref country code: EE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180103

Ref country code: RO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180103

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180103

Ref country code: CZ

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180103

Ref country code: SM

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180103

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180103

26N No opposition filed

Effective date: 20181005

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180103

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20181120

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20181120

Ref country code: MC

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180103

REG Reference to a national code

Ref country code: BE

Ref legal event code: MM

Effective date: 20181130

REG Reference to a national code

Ref country code: IE

Ref legal event code: MM4A

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20181130

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20181130

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20181120

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20181130

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20181120

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MT

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20181120

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: TR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180103

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20180103

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: HU

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT; INVALID AB INITIO

Effective date: 20141120

Ref country code: MK

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20180103

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20230929

Year of fee payment: 10

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20230929

Year of fee payment: 10